Promega Corporation
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2025-11-05
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| PMA | P240026 | Nucleic Acid Based Assay, Microsatellite Instability | SFL | 2025-11-05 | View |
| 510(k) | K200129 | OncoMate MSI Dx Analysis System | PZJ | 2021-07-26 | View |
No matching devices.