ClearanceBrief
510(k) K954871 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

LAPAROSCOPIC INSTRUMENT GROUNDING SYSTEM

ApplicantConmedcorp, Dayton OH, US
DecisionSubstantially Equivalent, Nov 2, 1995
ReceivedOct 24, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K954871

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.