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  2. Baroreflex activation therapy - Wikipedia

    en.wikipedia.org/wiki/Baroreflex_activation_therapy

    In common with pacemakers, implantation of baroreflex activation therapy devices carries risks of bleeding, bruising and infection. [2] High stimulation voltages can cause an appreciable sensation which can be unpleasant. In typical use the device output voltage is adjusted to below the level that causes unpleasant sensations. [3]

  3. Eko Health Inc. - Wikipedia

    en.wikipedia.org/wiki/Eko_Health_Inc.

    In 2018, Eko's low ejection fraction screening algorithm, developed with the Mayo Clinic, received a ‘Breakthrough Device’ designation from the FDA. [6] In 2020, Eko announced $65 million in funding, [7] and a collaboration with 3M. [8] Eko raised an additional $30M in funding in 2022, [9] and received FDA clearance for its murmur analysis ...

  4. MAKO Surgical Corp. - Wikipedia

    en.wikipedia.org/wiki/MAKO_Surgical_Corp.

    MAKO Surgical was founded in 2004 by Rony Abovitz and other key members of its predecessor Z-KAT, Inc. [9] Z-KAT was founded in 1997 by Rony Abovitz, William Tapia, Michael Peshkin Ph.D., Julio Santos-Munne, and Wayne J. Kerness, M.D. and was developing a novel haptic robotic system for medical applications, amongst a wide variety of computer-assisted surgery technologies.

  5. Oakland clinic gets medical device maker to disclose risk of ...

    www.aol.com/news/oakland-clinic-gets-medical...

    When Dr. Noha Aboelata learned that research stretching back decades showed that pulse oximeters routinely failed patients with darker skin, she took action.

  6. Frequency specific microcurrent - Wikipedia

    en.wikipedia.org/wiki/Frequency_specific_micro...

    A 1994 review of electronic devices as potential cancer treatments by the American Cancer Society found the methods to questionable, ineffective, and strongly advises against using them. [ 4 ] Another criticism is that the champion of the modality is a discredited chiropractor.

  7. FDA Center for Devices and Radiological Health - Wikipedia

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

    The 2002 Medical Device User Fee and Modernization Act (MDUFA) first granted FDA the authority to collect user fees from industry to help the FDA improve efficiency, quality, and predictability of medical device submission reviews; the medical device user fee program has been reauthorized several times with the most recent in 2022.

  8. Proton therapy - Wikipedia

    en.wikipedia.org/wiki/Proton_therapy

    In medicine, proton therapy, or proton radiotherapy, is a type of particle therapy that uses a beam of protons to irradiate diseased tissue, most often to treat cancer.The chief advantage of proton therapy over other types of external beam radiotherapy is that the dose of protons is deposited over a narrow range of depth; hence in minimal entry, exit, or scattered radiation dose to healthy ...

  9. FDA approves new pain medication as an alternative to ... - AOL

    www.aol.com/fda-approves-pain-medication...

    For the first time in two decades, the Food and Drug Administration (FDA) has approved a new class of medication that provides an alternative to addictive opioids for patients looking to manage ...