ClearanceBrief
510(k) K240537 ยท GEX Powered Laser Surgical Instrument

SMARTXIDE PRO

ApplicantEl.En S.P.A., Calenzano, IT
DecisionSubstantially Equivalent, Mar 20, 2024
ReceivedFeb 26, 2024
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K240537

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.