ClearanceBrief
510(k) K813356 ยท FNJ Bed, Manual

DEVICE FOR REPOSITIONING A BET PATIENT

ApplicantAli-Oop Co., Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 10, 1982
ReceivedNov 27, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K813356

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.