Sutter Medizintechnik GmbH
9 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| CURIS II RF Generator (REF 360100-05) (K251813) | Sutter Medizintechnik GmbH | 2026-02-11 |
| FlexTip Bipolar electrodes single-use (AR-S9805-0028), FlexTip Bipolar electrodes single-use (AR-S9805-0035) (K233425) | Sutter Medizintechnik GmbH | 2024-01-25 |
| Sutter Swyng non-stick bipolar forceps, single-use (K193587) | Sutter Medizintechnik GmbH | 2020-02-10 |
| Sutter Arrowtip Monopolar Electrodes (K192128) | Sutter Medizintechnik GmbH | 2019-10-04 |
| Sutter RaVoR Bipolar Electrodes (K191732) | Sutter Medizintechnik GmbH | 2019-08-30 |
| Sutter CURIS RF Generator (K171869) | Sutter Medizintechnik GmbH | 2018-02-23 |
| Sutter Bipolar Forceps-Calvian (K150959) | Sutter Medizintechnik GmbH | 2015-09-10 |
| SUTTER BIPOLAR FORCEPS - SUPERGLISS (K131012) | Sutter Medizintechnik GmbH | 2013-08-23 |
| SUTTER ELECTROSURGICAL CABLES (K073450) | Sutter Medizintechnik GmbH | 2008-03-17 |
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Every clearance here is in the API, with alerts when new ones post.