ClearanceBrief
510(k) K202980 ยท GEX Powered Laser Surgical Instrument

Laser Therapy Device

ApplicantShenzhen Leaflife Technology Co., Ltd., Shenzhen, CN
DecisionSubstantially Equivalent, Nov 19, 2020
ReceivedSep 30, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K202980

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.