ClearanceBrief
510(k) K943481 ยท KMI Monitor, Bed Patient

INFORMER PLUS

ApplicantMicro-Tech Medical, Inc., East Hartford CT, US
DecisionSubstantially Equivalent, Nov 2, 1994
ReceivedJul 19, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K943481

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.