ClearanceBrief
510(k) K926045 ยท FNM Mattress, Air Flotation, Alternating Pressure

SKYTRON LIFE ISLAND 21

ApplicantSkytron, Div. the Kmw Group, Inc., Grand Rapids MI, US
DecisionSubstantially Equivalent, Jul 27, 1993
ReceivedDec 1, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K926045

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.