Medical Device Manufacturer · US , Redwood City , CA

Myoscience, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2009

Total

Cleared

Denied

Myoscience, Inc. has 9 FDA 510(k) cleared medical devices. Based in Redwood City, US.

Historical record: 9 cleared submissions from 2009 to 2018. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Myoscience, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Myoscience, Inc.

9 devices

1-9 of 9

Myoscience iovera system

MYOSCIENCE CRYO-TOUCH

K100447 · GXH

Neurology · 128d

Cleared Mar 20, 2009

MYOSCIENCE CRYO-TOUCH

K083493 · GEH

General & Plastic Surgery · 115d

Myoscience, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Myoscience, Inc.

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