ClearanceBrief
510(k) K192103 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

Thunderbeat Open Fine Jaw Type X Hand Instrument

ApplicantOlympus Medical Systems Corp., Hachioji-Shi, JP
DecisionSubstantially Equivalent, May 11, 2020
ReceivedAug 5, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K192103

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.