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New 510(k) boosts iRhythm, Verily efforts for AFib screening

January 24, 2020 By Chris Newmarker

Verily’s Study Watch [Image courtesy of Verily]

The latest 510(k) clearance for the Verily Study Watch will further the efforts of the Google sister company and iRhythm Technologies (NSDQ:IRTC)  to improve atrial fibrillation treatment.

Verily — a life science company under Alphabet (NSDQ:GOOGL) — recently received an FDA 510(k) clearance to include an irregular pulse monitor in its Study Watch wearable.

“We’ve worked carefully to meet the FDA’s stringent requirements for medical devices, and with this new indication, will explore opportunities to leverage Study Watch as a measure of irregular pulse in clinical settings across our cardiovascular programs, including our collaboration with iRhythm,” Dr. William Marks, head of clinical science at Verily, said in a blog post yesterday.

Get the full story on our sister site, MassDevice.

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  • Home
  • Medical Device Business
    • Mergers & Acquisitions
    • Financial
    • Regulatory
  • Applications
    • Cardiovascular
    • Devices
    • Imaging
    • Implantables
    • Medical Equipment
    • Orthopedic
    • Surgical
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    • Contract Manufacturing
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    • Electronics
    • Extrusions
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    • Motion Control
    • Prototyping
    • Pumps
    • Tubing
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  • 2022 Leadership in MedTech
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