Sutter Medizintechnik GmbH
FDA 510(k) & PMA Approved Devices — 6 products
Total Devices6
Categories1
Latest FDA decision2026-02-11
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K251813 | CURIS II RF Generator (REF 360100-05) | GEI | 2026-02-11 | View |
| 510(k) | K233425 | FlexTip Bipolar electrodes single-use (AR-S9805-0028), FlexTip Bipolar electrodes single-use (AR-S9805-0035) | GEI | 2024-01-25 | View |
| 510(k) | K193587 | Sutter Swyng non-stick bipolar forceps, single-use | GEI | 2020-02-10 | View |
| 510(k) | K192128 | Sutter Arrowtip Monopolar Electrodes | GEI | 2019-10-04 | View |
| 510(k) | K191732 | Sutter RaVoR Bipolar Electrodes | GEI | 2019-08-30 | View |
| 510(k) | K171869 | Sutter CURIS RF Generator | GEI | 2018-02-23 | View |
No matching devices.