ClearanceBrief
510(k) K852036 ยท INX Bed, Air Fluidized

AIR PLUS AIR FLUIDIZED THERAPY SYSTEMS

ApplicantAir Plus, Inc., Miami FL, US
DecisionSubstantially Equivalent, Sep 5, 1985
ReceivedMay 9, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K852036

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.