ClearanceBrief
510(k) K220381 ยท GEX Powered Laser Surgical Instrument

Diode Laser Therapy Systems

ApplicantBeijing Lasertell Medical Co., Ltd., Beijing, CN
DecisionSubstantially Equivalent, May 20, 2022
ReceivedFeb 10, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220381

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.