Medical Device Manufacturer · US , Pleasanton , CA

Zeltiq Aesthetics - FDA 510(k) Cleared Devices

4 submissions · 3 cleared · Since 2008

Total

Cleared

Denied

Zeltiq Aesthetics has 3 FDA 510(k) cleared medical devices. Based in Pleasanton, US.

Historical record: 3 cleared submissions from 2008 to 2017. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Zeltiq Aesthetics

4 devices

1-4 of 4