ClearanceBrief
510(k) K220103 ยท GEX Powered Laser Surgical Instrument

LED Therapy Device (Planar LED/Planar LED mini)

ApplicantShenzhen Leaflife Technology Co., Ltd., Shenzhen, CN
DecisionSubstantially Equivalent, Apr 12, 2022
ReceivedJan 12, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220103

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.