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  2. Medtronic Shares Fall After FDA Warning Letter To Its ... - AOL

    www.aol.com/news/medtronic-shares-fall-fda...

    Medtronic Plc (NYSE: MDT) received a warning letter from the FDA highlighting certain concerns related to medical device quality requirements at the Company's diabetes business headquarters. The ...

  3. Medtronic Wins FDA Approval for MRI-Accessible Pacemaker - AOL

    www.aol.com/news/2013-02-14-medtronic-wins-fda...

    Medical device maker Medtronic announced in a press release yesterday that it has won FDA regulatory approval for its Advisa DR MRI SureScan pacemaker. The Advisa is Medtronic's second MR ...

  4. Safety of magnetic resonance imaging - Wikipedia

    en.wikipedia.org/wiki/Safety_of_magnetic...

    All patients are reviewed for contraindications prior to MRI scanning. Medical devices and implants are categorized as MR Safe, MR Conditional or MR Unsafe: [6] MR-Safe – The device or implant is completely non-magnetic, non-electrically conductive, and non-RF reactive, eliminating all of the primary potential threats during an MRI procedure.

  5. FDA recalls close to half-a-million pacemakers over ... - AOL

    www.aol.com/news/2017-08-31-fda-pacemakers...

    At least if you have a pacemaker, that is. On Tuesday, the FDA recalled 465,000 of the medical devices -- the ones that help control your heart beat -- citing security vulnerabilities.

  6. Artificial cardiac pacemaker - Wikipedia

    en.wikipedia.org/wiki/Artificial_cardiac_pacemaker

    As of 2014 the five most commonly used cardiac pacing device manufacturers (covering more than 99% of the US market) made FDA-approved MR-conditional pacemakers. [34] The use of MRI may be ruled out by the patient having an older, non-MRI Conditional pacemaker, or by having old pacing wires inside the heart, no longer connected to a pacemaker.

  7. Pacemaker failure - Wikipedia

    en.wikipedia.org/wiki/Pacemaker_failure

    The magnet can interrupt the pacing and inhibit the output of pacemakers. If MRI must be done, the pacemaker output in some models can be reprogrammed. [7] In February 2011, the FDA approved an MRI-safe pacemaker. [8] Extracorporeal shock-wave lithotripsy (ESWL) procedure is safe for most pacemaker patients, with some reprogramming of the pacing.

  8. Medtronic Recalls Some Versions Of Software Used For ... - AOL

    www.aol.com/medtronic-recalls-versions-software...

    Medtronic Plc (NYSE:MDT) has initiated a recall for some versions of its StealthStation S8 application. The FDA deemed software recall as Class I, the most serious kind. The medical device giant ...

  9. 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]

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