ClearanceBrief
510(k) K062312 ยท GEX Powered Laser Surgical Instrument

AXIOM PULSED LIGHT SYSTEM

ApplicantGeneral Project S.R.L., Stamford CT, US
DecisionSubstantially Equivalent, Oct 16, 2006
ReceivedAug 8, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K062312

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.