ClearanceBrief
510(k) K904008 ยท INX Bed, Air Fluidized

STAGE IV, AIR-FLUIDIZE BED

ApplicantUnique Flotation Systems, Inc., Corona CA, US
DecisionSubstantially Equivalent, Oct 10, 1990
ReceivedAug 29, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K904008

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.