ClearanceBrief
510(k) K872358 ยท KMI Monitor, Bed Patient

STA-PUT

ApplicantDesign Technologies, Inc., Rahway NJ, US
DecisionSubstantially Equivalent, Aug 6, 1987
ReceivedJun 18, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K872358

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.