ClearanceBrief
510(k) K840295 ยท KMI Monitor, Bed Patient

AMBULARM

ApplicantRigi Systems, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, May 7, 1984
ReceivedJan 24, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K840295

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.