ClearanceBrief
510(k) K020067 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

GYRUS ENT SOMNOPLASTY GENERATOR

ApplicantGyrus Ent LLC, Bartlett TN, US
DecisionSubstantially Equivalent, Apr 4, 2002
ReceivedJan 9, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K020067

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.