510(k) K191234 · GEI Electrosurgical, Cutting & Coagulation & Accessories

APC 3 Argon Plasma Coagulation Unit, VIO 3 Electrosurgical Unit, FiAPC probes, Hybrid APC, APCapplicators, APC Pressure Reducer with Sensor, VIO Cart, Fastening sets

Applicant	Erbe Elektromedizin GmbH, Tuebingen, DE
Decision	Substantially Equivalent, Dec 20, 2019
Received	May 8, 2019
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K191234

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.