Lifecell Corporation
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories2
Latest Approval2020-05-28
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K193539 | REVOLVE ENVI 600 Advanced Adipose System | MUU | 2020-05-28 | View |
| 510(k) | K163647 | Revolve Envi 600 Advanced Adipose System | MUU | 2017-08-25 | View |
| 510(k) | K162752 | ARTIA Reconstructive Tissue Matrix Perforated | FTM | 2017-02-24 | View |
No matching devices.