ClearanceBrief
510(k) K031993 ยท GEX Powered Laser Surgical Instrument

AURORA SR

ApplicantSyneron Medical, Ltd., Yoqneam Illit, IL
DecisionSubstantially Equivalent, Aug 1, 2003
ReceivedJun 27, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K031993

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.