ClearanceBrief
510(k) K231791 ยท GEX Powered Laser Surgical Instrument

PENTO Nd:YAG and Alexandrite laser system

ApplicantIlooda Co,., Ltd., Anyang-Si, KR
DecisionSubstantially Equivalent, Sep 15, 2023
ReceivedJun 20, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K231791

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.