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From: "Equity Alert Center" <Alerts@Alerts.EquityAlert.com>
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Subject: OUR LAST ALERT - UP 29 % => THIS WEEK - RUBICON MEDICAL (RMDC)
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Date: 7 Aug 2002 18:57:47 -0700

Special Situations Alert

www.equityalert.com
OUR LAST ALERT - UP 29 %
THIS WEEK RUBICON MEDICAL (RMDC)

  • Our last Special Situations Alert gained 29% immediately after our introduction. This week, we present RUBICON MEDICAL, INC. (OTC BB: RMDC) named as one of the TOP 100 public companies by Utah business (May 2002).
     
  • RMDC has developed some of the most advanced patented medical devices that treat and prevent complications in interventional cardiology, radiology and peripheral interventional radiology a $1 Billion market!

  • RMDC has already licensed its technology to Abbott Labs (NYSE: ABT) in a deal worth almost 30 cents a share to the company !! Amazingly, RMDC trades at just 40 cents per share !

  • With other significant products in the pipeline, 756% annual increase in revenues since 1999, experienced management and a relatively low priced stock, watch for strong investor interest in RMDC in the near future.


    www.equityalert.com

      EQ

    Rubicon Medical Announces Plans for a CE Mark Clinical Study
    To Obtain Regulatory Approval in Europe for the Rubicon Filter

    SALT LAKE CITY, Aug. 5 /PRNewswire-FirstCall/ -- Rubicon Medical Corporation (OTC Bulletin Board: RMDC), a developer and manufacturer of medical devices and products, today announced plans for a CE Mark clinical study of the Rubicon Filter in Europe. The study will test the Rubicon Filter in saphenous vein grafts (SVGs), which are degenerated coronary bypass grafts in which blockages have reappeared following heart bypass surgery. The CE Mark is the regulatory approval that must be obtained in order to market a medical device in the European Union.

    "We will soon begin the process for regulatory approval of the Rubicon Filter in the European Union for SVG patients. Our research and development team has worked under an accelerated schedule, and we plan to commence clinical studies in either the 4th quarter of 2002, or 1st quarter of 2003. These studies are anticipated to take 3-4 months to complete," stated Mr. Richard J. Linder, Rubicon President and CEO. Linder also noted that "We have completed feasibility testing at the Utah Artificial Heart Institute, and we plan to begin the FDA approval process after the CE Mark studies have been completed."

    The Rubicon Filter is an embolic filter, a medical device designed to be inserted into a blood vessel and allow blood to continue flowing during a surgical procedure, while blocking any particle large enough to cause damage to the body. During many coronary vascular procedures, a principal risk is that plaque material from a coronary blockage can be dislodged to travel through the body. Such loose particles can block other blood vessels (a condition called embolization) and cause a stroke, heart attack or other very serious problem. The Rubicon Filter is designed to prevent or reduce the possibility of serious or fatal embolization caused by such loose particles. In addition, the Rubicon Filter is the smallest known embolic protection filter device in existence. Although similar devices currently are in use in other countries, no other filter device similar to the Rubicon Filter has yet been approved for use in the United States. When inserted into a coronary artery past an atherosclerotic (plaque) blockage, the Rubicon Filter's extremely small size will greatly reduce the risk of breaking free particles that can cause serious injury to the patient during passage of the filter.

    The Rubicon Filter's small size also means it will be much simpler and easier for surgeons to navigate it through coronary arteries. Rubicon believes that the filter's advanced features and ease of use will present a significant improvement for interventional physicians over existing filter technologies marketed by Boston Scientific, Guidant, Medtronic and Cordis (Johnson & Johnson). The worldwide market for embolic protection devices such as the Rubicon Filter is estimated at a potential $1 billion dollars annually.

    "The commencement of European studies re-affirms our commitment to conduct our own clinical studies, grow our business and to market our own proprietary technologies worldwide. We believe that once we obtain regulatory approvals, the Rubicon Filter will become a standard choice of interventional physicians," Mr. Linder continued.

    Randall Higashida, MD, Rubicon's Medical Director, stated: "I am very excited with the efforts Rubicon has invested in the Rubicon Filter for SVG patients. The Rubicon Filter, once approved in the U.S. and Europe, holds the potential to make these coronary procedures safer for SVG patients, and we intend to establish this through clinical research." Dr. Higashida is the Chief of Interventional Neuro-Radiology at the University of California at San Francisco, President of the American Society of Interventional Therapeutic Neuroradiology (ASITN), and Chairman of the American Heart Association's Committee on Cerebrovascular Disease.

    About Rubicon Medical

    Rubicon Medical Corporation is a Salt Lake City-based developer and manufacturer of interventional vascular medical devices and products. The Company focuses on minimally invasive endovascular techniques and products that are safer and more cost effective than surgery. Rubicon was proud to be named one of the Top 100 Utah public companies by Utah Business magazine in May 2002.

    Rubicon has licensed a different embolic protection product, the Guardian system, to Abbott Laboratories, which will conduct the FDA regulatory approval process for the Guardian in the United States and also the CE Mark clinical study program in Europe.

    Forward-Looking

    Statements
    All forward-looking statements in this release are based upon information available to the Company on the date of this release. Any forward-looking statements involve risks and uncertainties, including those risks and uncertainties described in the Company's filings with the Securities and Exchange Commission, that could cause actual events or results to differ materially from the events or results described in the forward-looking statements, whether as a result of new information, future events or otherwise. The Rubicon Filter and Guardian devices have not yet been approved for sale in the U.S. or Europe, and no assurance exists that such approvals will be obtained; Readers should not place undue reliance on these forward-looking statements.





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We are not responsible for the reliability of these external sites nor are we responsible for any of the contents, advertising, products, or other materials on such external sites. EQOur inclusion of hyperlinks to such web sites does not imply any endorsement of the material on such web sites or any association with their operators. Under no circumstances shall we be held responsible or liable, directly or indirectly, for any loss or damage caused or alleged to have been caused in connection with the use of or reliance on any content, goods, or services available on such external site. Any concerns regarding any external link should be directed to its respective site administrator or webmaster. We may refer to other sources of information, or other commentary. We intend to offer these items to readers as additional sources of information, but disclaim any implication that we endorse information contained in such outside sources. 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