ClearanceBrief
510(k) K060484 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ERBE VIO ESU, MODEL VIO 300 D

ApplicantErbe USA, Inc., Alpharetta GA, US
DecisionSubstantially Equivalent, Mar 16, 2006
ReceivedFeb 24, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K060484

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.