Prowess, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
Advertisement
Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K231825 | Panther TPS | MUJ | 2023-12-15 | View |
| 510(k) | K211760 | Panther OIS | IYE | 2021-09-28 | View |
| 510(k) | K193459 | Panther Stereotactic | MUJ | 2020-04-27 | View |
| 510(k) | K122616 | PANTHER OIS/R & V MODEL VERSION 2.0 | IYE | 2012-12-21 | View |
| 510(k) | K101076 | PROWESS PANTHER PROARC, MODEL VERSION 5.0 | MUJ | 2010-07-27 | View |
| 510(k) | K100801 | PUMA MODEL VERSION 1.0 | IYE | 2010-06-18 | View |
| 510(k) | K083502 | PANTHER REALART, MODEL 4.7 | MUJ | 2009-05-05 | View |
| 510(k) | K032456 | PROWESS | MUJ | 2003-10-16 | View |
No matching devices.
Advertisement