ClearanceBrief
510(k) K100224 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ESTECH COBRA BIPOLSR II

ApplicantEndoscopic Technologies, Inc. D/B/A Estech, San Ramon CA, US
DecisionSubstantially Equivalent, Apr 7, 2010
ReceivedJan 26, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K100224

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.