ClearanceBrief
510(k) K924686 ยท INX Bed, Air Fluidized

REM-AIR

ApplicantMellenair Ent., Inc., Long Beach CA, US
DecisionSubstantially Equivalent, Feb 12, 1993
ReceivedSep 16, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K924686

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.