Erbe Elektromedizin GmbH
Erbe Elektromedizin GmbH holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2026.
Top product codes for Erbe Elektromedizin GmbH
Recent clearances by Erbe Elektromedizin GmbH
- K261806 — ERBECRYO 2 Cryosurgical Unit and Accessories
- K253230 — ERBECRYO 2 Cryosurgical Unit and Accessories: ERBECRYO 2 cryosurgical unit; Erbe Flexible Cryoprobe
- 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 +4 more
- 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.