ClearanceBrief
510(k) K010265 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

BAYLIS MEDICAL RF PERFORATION PROBE, MODEL RFP-265

ApplicantBaylis Medical Co., Inc., Mississauga, Ontario, CA
DecisionSubstantially Equivalent, Apr 9, 2001
ReceivedJan 26, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K010265

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.