ClearanceBrief
510(k) K905752 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ARGON BEAM COMBO LAPAROSCOPIC ELECTRODE

ApplicantBeacon Laboratories, Inc., Broomfield CO, US
DecisionSubstantially Equivalent, Jul 22, 1991
ReceivedDec 24, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K905752

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.