ClearanceBrief
510(k) K123141 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ENSEAL TRIO TISSUE SEALING DEVICE

ApplicantEthicon Endo-Surgery, LLC, Cincinnati OH, US
DecisionSubstantially Equivalent, Oct 25, 2012
ReceivedOct 5, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K123141

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.