ClearanceBrief
510(k) K232645 ยท FRA Purifier, Air, Ultraviolet, Medical

Airgle Room Air Purifier

ApplicantAirgle Corporation, Holbrook NY, US
DecisionSubstantially Equivalent, Feb 16, 2024
ReceivedAug 30, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232645

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.