ClearanceBrief
510(k) K885200 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

600 & 900 SERIES ELECTRODES & 755 & 756 HANDLE

ApplicantOlsen Electrosurgical, Inc., Concord CA, US
DecisionSubstantially Equivalent, Jan 13, 1989
ReceivedDec 16, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K885200

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.