Medical Device Manufacturer · US , Menlo Park , CA

Cabochon Aesthetics, Inc. - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 2013

Total

Cleared

Denied

Cabochon Aesthetics, Inc. has 1 FDA 510(k) cleared medical devices. Based in Menlo Park, US.

Historical record: 1 cleared submissions from 2013 to 2014. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Cabochon Aesthetics, Inc.

2 devices

1-2 of 2