ClearanceBrief
510(k) K130596 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

CAIMAN SEAL AND CUT TECHNOLOGY

ApplicantAesculap, Inc., Center Valley PA, US
DecisionSubstantially Equivalent, Mar 22, 2013
ReceivedMar 7, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K130596

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.