ClearanceBrief
510(k) K162075 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

NICO TRIOwand

ApplicantNico Corporation, Indianapolis IN, US
DecisionSubstantially Equivalent, Aug 11, 2016
ReceivedJul 27, 2016
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K162075

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.