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.

Zeltiq Aesthetics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Zeltiq Aesthetics

4 devices

1-4 of 4