ClearanceBrief
510(k) K992382 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

SURGITRON RADIOLASE

ApplicantEllman Intl., Inc., Hewlett NY, US
DecisionSubstantially Equivalent, Oct 14, 1999
ReceivedJul 16, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K992382

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.