ClearanceBrief
510(k) K232709 ยท GEX Powered Laser Surgical Instrument

Diode laser therapy device

ApplicantHebei Zhemai Technology Co., Ltd., Langfang, CN
DecisionSubstantially Equivalent, Nov 30, 2023
ReceivedSep 5, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232709

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.