ClearanceBrief
510(k) K132374 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

BAYLIS MEDICAL RF PERFORATION PROBE V2.0

ApplicantBaylis Medical Company, Inc., Mississauga, Ontario, CA
DecisionSubstantially Equivalent, Aug 30, 2013
ReceivedJul 30, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K132374

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.