ClearanceBrief
510(k) K874877 ยท FNM Mattress, Air Flotation, Alternating Pressure

PEGASUS AIRWAVE SYST/SPEC MATTRESS DECUBITUS ULCER

ApplicantPegasus Airwave, Inc., Hants Po35qt, England, GB
DecisionSubstantially Equivalent, Feb 22, 1988
ReceivedNov 13, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K874877

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.