ClearanceBrief
510(k) K103032 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ESG-400 MODEL WB95051N, FOOTSWITCH DOUBLE PEDAL MODEL WB50402W, FOOTSWITCH SINGLE PEDAL MODEL WB50403W, P-CORD MODEL MAJ

ApplicantOlympus Winter & Ibe GmbH, Center Valley PA, US
DecisionSubstantially Equivalent, Jan 14, 2011
ReceivedOct 12, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K103032

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.