ClearanceBrief
510(k) K122278 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

BAYLIS MEDICAL COMPANY RADIOFREQUENCY PERFORATION GENERATOR

ApplicantBaylis Medical Company, Inc., Mississauga, Ontario, CA
DecisionSubstantially Equivalent, Nov 7, 2012
ReceivedJul 30, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K122278

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.