ClearanceBrief
510(k) K933552 ยท KMI Monitor, Bed Patient

PM-PAGER

ApplicantHill Engineering, Boxford MA, US
DecisionSubstantially Equivalent, Sep 22, 1994
ReceivedJul 21, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K933552

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.