ClearanceBrief
510(k) K934689 ยท INX Bed, Air Fluidized

LOW AIR LOSS MATTRESS, MODIFICATION

ApplicantCardio Systems, Inc., Dallas TX, US
DecisionSubstantially Equivalent, Feb 2, 1994
ReceivedAug 23, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K934689

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.