ClearanceBrief
510(k) K140388 ยท GEX Powered Laser Surgical Instrument

LUMENIS PULSE 120H

ApplicantLumenis, Ltd., Ramat Gan, IL
DecisionSubstantially Equivalent, Mar 14, 2014
ReceivedFeb 14, 2014
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K140388

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.