Sutter Medizintechnik GmbH - FDA 510(k) Cleared Devices
Recent clearances: CURIS II RF Generator (REF 360100-05), FlexTip Bipolar electrodes single-use (AR-S9805-0028), FlexTip Bipolar electrodes single-use (AR-S9805-0035), Sutter Swyng non-stick bipolar forceps, single-use
9
Total
9
Cleared
0
Denied
FDA 510(k) Regulatory Record - Sutter Medizintechnik GmbH Ear, Nose, Throat ✕
1 devices