ClearanceBrief
510(k) K023886 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ERBE VIO ESU WITH ACCESSORIES, MODEL VIO 300 D

ApplicantErbe USA, Inc., Marietta GA, US
DecisionSubstantially Equivalent, Dec 12, 2002
ReceivedNov 21, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K023886

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.