ClearanceBrief
510(k) K221363 ยท PDZ Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis

AF Laser

ApplicantShenB Co., Ltd., Seoul, KR
DecisionSubstantially Equivalent, Jul 20, 2022
ReceivedMay 11, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K221363

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.