ClearanceBrief
510(k) K120791 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

AMBIENT TURBOFLASH 90 IFS

ApplicantArthocare Corporation, Austin TX, US
DecisionSubstantially Equivalent, Dec 11, 2012
ReceivedMar 15, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K120791

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.