Erbe Elektromedizin GmbH
FDA 510(k) medical device clearances.
Top product codes for Erbe Elektromedizin GmbH
Recent clearances by Erbe Elektromedizin GmbH
- K253915 — MOVIVA® Hybrid Ablation Probe
- K251108 — Erbe ESU Model VIO® 3n with Accessories
- K243120 — HybridAPC probe
- K243451 — FiAPC plus probes
- K242044 — FiAPC plus probes
- K240932 — HybridTherm System
- K232033 — HYBRIDknife® flex
- K231023 — ERBEJET® 2 System
- K190651 — ERBECRYO 2 Cryosurgical Unit; ERBECRYO 2 1-pedal footswitch, Extension cable f. ERBECRYO 2 footswitch; Flexible Cryoprobe; ERBECRYO 2 Cart, VIO-Cart, Wire basket; Connecting hoses, switching valves, adapter
- K191234 — APC 3 Argon Plasma Coagulation Unit, VIO 3 Electrosurgical Unit, FiAPC probes, Hybrid APC, APCapplicators, APC Pressure Reducer with Sensor, VIO Cart, Fastening sets
- K190823 — Erbe ESU Model VIO 3 with Accessories
- K183445 — Erbe APCapplicators
- K150364 — ERBE ESU Model VIO dV with Accessories
- K934261 — ERBOKRYO CA CRYOSURGICAL SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.