Progenika Biopharma S.A., A Grifols Company
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories2
Latest FDA decision2022-10-27
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K221420 | AlphaID™ At Home Genetic Health Risk Service | PTA | 2022-10-27 | View |
| 510(k) | K211115 | A1AT Genotyping Test | PZH | 2021-05-13 | View |
| 510(k) | K192858 | A1AT Genotyping Test | PZH | 2019-11-05 | View |
| 510(k) | K171868 | A1AT Genotyping Test | PZH | 2017-11-11 | View |
No matching devices.