ClearanceBrief
510(k) K841671 ยท KMI Monitor, Bed Patient

FALL-SAFE MONITOR

ApplicantFsm Corp., Walker MI, US
DecisionSubstantially Equivalent, Jul 3, 1984
ReceivedApr 23, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K841671

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.