ClearanceBrief
510(k) K083452 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ERBE MODEL VIO 300 D WITH ACCESSORIES

ApplicantErbe USA, Inc., Alpharetta GA, US
DecisionSubstantially Equivalent, Dec 31, 2008
ReceivedNov 21, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K083452

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.