ClearanceBrief
510(k) K944310 ยท FNM Mattress, Air Flotation, Alternating Pressure

PEGASUS BIWAVE PLUS SYSTEM

ApplicantPegasus Airwave, Inc., Deerfield Beach FL, US
DecisionSubstantially Equivalent, Mar 17, 1995
ReceivedSep 2, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K944310

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.