ClearanceBrief
510(k) K960009 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

STORZ S2050 SERIES BIPOLAR FORCEPS

ApplicantStorz Instrument Co., St. Louis MO, US
DecisionSubstantially Equivalent, Mar 6, 1996
ReceivedJan 2, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960009

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.