Zeltiq Aesthetics, Inc.
FDA 510(k) & PMA Approved Devices — 9 products
Total Devices9
Categories2
Latest Approval2024-02-01
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K233804 | Resonic Rapid Acoustic Pulse Device | GEX | 2024-02-01 | View |
| 510(k) | K222629 | Resonic Rapid Acoustic Pulse Device | GEX | 2022-09-25 | View |
| 510(k) | K212707 | CoolSculpting Elite System | OOK | 2021-11-05 | View |
| 510(k) | K193566 | ZELTIQ CoolSculpting System | OOK | 2020-01-21 | View |
| 510(k) | K183514 | ZELTIQ CoolSculpting System | OOK | 2019-01-14 | View |
| 510(k) | K181740 | ZELTIQ CoolSculpting System | OOK | 2018-08-29 | View |
| 510(k) | K171069 | ZELTIQ CoolSculpting System | OOK | 2017-07-07 | View |
| 510(k) | K162050 | ZELTIQ CoolSculpting System | OOK | 2016-11-21 | View |
| 510(k) | K160259 | ZELTIQ CoolSculpting System | OOK | 2016-03-23 | View |
No matching devices.