ClearanceBrief
510(k) K926403 ยท FNM Mattress, Air Flotation, Alternating Pressure

PRO-2000 LOW AIR LOSS THERAPY BED

ApplicantCh Administration, Inc., Dallas TX, US
DecisionSubstantially Equivalent, Jul 30, 1993
ReceivedDec 21, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K926403

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.