ClearanceBrief
510(k) K901096 ยท FNM Mattress, Air Flotation, Alternating Pressure

LUMISCOPE ALTERNATING PRESSURE PAD & PUMP

ApplicantLumiscope Co., Inc., Edison NJ, US
DecisionSubstantially Equivalent, Aug 21, 1990
ReceivedMar 7, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901096

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.