ClearanceBrief
510(k) K231950 ยท GEX Powered Laser Surgical Instrument

MEDIDIODE

ApplicantMedicreations, LLC, Las Vegas NV, US
DecisionSubstantially Equivalent, Aug 9, 2024
ReceivedJun 30, 2023
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K231950

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.