Medical Device Manufacturer · US , Menlo Park , CA

Miramar Labs, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2009

Total

Cleared

Denied

Miramar Labs, Inc. has 6 FDA 510(k) cleared medical devices. Based in Menlo Park, US.

Historical record: 6 cleared submissions from 2009 to 2018. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Miramar Labs, Inc.

6 devices

1-6 of 6