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  2. Medtronic faces FDA Class I recall for post-op drainage device

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    The U.S. Food and Drug Administration has issued a Class I recall, the agency's most serious, for a Medtronic device used to temporarily drain spinal fluid from patients after surgery for a ...

  3. Medtronic's (MDT) HVAD Pump Kit Recall Classified as Class I

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  4. Medtronic - Wikipedia

    en.wikipedia.org/wiki/Medtronic

    Medtronic operational headquarters in Fridley, Minnesota, a suburb of Minneapolis. Medtronic was founded in 1949 in Minneapolis by Earl Bakken and his brother-in-law, Palmer Hermundslie, as a medical equipment repair shop. [8] Bakken invented several medical technology devices that continue to be used around the world today. [citation needed]

  5. Medtronic's StealthStation Feature Recall Classified Class I

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  6. Product recall - Wikipedia

    en.wikipedia.org/wiki/Product_recall

    A product recall is a request from a manufacturer to return a product after the discovery of safety issues or product defects that might endanger the consumer or put the maker or seller at risk of legal action. Product recalls are one of a number of corrective actions that can be taken for products that are deemed to be unsafe.

  7. Gary K. Michelson - Wikipedia

    en.wikipedia.org/wiki/Gary_K._Michelson

    In 2005, Michelson sold many of his spine-related patents to Medtronic for $1.35 billion, [13] placing him on the Forbes 400 list. [14] A legal battle with Medtronic over the origins of the patents preceded the sale. In 2004, Michelson cross-filed in response to Medtronic's 2001 suit, and was awarded financial damages for both lawsuits by the ...

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    The search engine that helps you find exactly what you're looking for. Find the most relevant information, video, images, and answers from all across the Web.

  9. FDA Center for Devices and Radiological Health - Wikipedia

    en.wikipedia.org/wiki/FDA_Center_for_Devices_and...

    The MDA established a risk-based framework for the classification of medical devices and a regulatory pathway for medical devices to get to the market, created a regulatory pathway for medical device clinical trials, and established several post-market requirements including manufacturer registration and device listing with the FDA, good ...