Alliqua Biomedical, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2017-08-22
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K171041 | SilverSeal | FRO | 2017-08-22 | View |
| 510(k) | K162721 | Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator | NRB | 2016-12-22 | View |
No matching devices.