ClearanceBrief
510(k) K934344 ยท KMI Monitor, Bed Patient

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ApplicantMedway, Franklin TN, US
DecisionSubstantially Equivalent, Apr 29, 1994
ReceivedSep 8, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K934344

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.