ClearanceBrief
510(k) K083608 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ERBE HYBRID KNIFE

ApplicantErbe USA, Inc., Marietta GA, US
DecisionSubstantially Equivalent, Aug 26, 2009
ReceivedDec 5, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K083608

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.