ClearanceBrief
510(k) K140839 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

CAIMAN SEAL AND CUT TECHNOLOGY

ApplicantAesculap, Inc., Center Valley PA, US
DecisionSubstantially Equivalent, Apr 28, 2014
ReceivedApr 2, 2014
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K140839

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.