ClearanceBrief
510(k) K232642 ยท FRA Purifier, Air, Ultraviolet, Medical

AirKEE T900

ApplicantHealkee Medical Pte, Ltd., Singapore, SG
DecisionSubstantially Equivalent, May 23, 2024
ReceivedAug 30, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232642

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.