ClearanceBrief
510(k) K801517 ยท FNJ Bed, Manual

BED ROCKING DEVICE

ApplicantWesler, Walker MI, US
DecisionSubstantially Equivalent, Oct 10, 1980
ReceivedJul 1, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801517

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.