ClearanceBrief
510(k) K932632 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

CHAKOFF ENDOSCOPY LAPAROSCOPIC INSTRUMENTATION

ApplicantStephen Chakoff, Inc., Miami FL, US
DecisionSubstantially Equivalent, Jun 21, 1994
ReceivedJun 1, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K932632

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.