ClearanceBrief
510(k) K080715 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ERBE VIO ESU, MODEL VIO 200 S

ApplicantErbe USA, Inc., Marietta GA, US
DecisionSubstantially Equivalent, Apr 2, 2008
ReceivedMar 13, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K080715

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.