ClearanceBrief
510(k) K905113 ยท IKZ Bed, Patient Rotation, Powered

ROTO REST; TRAUMA AND INTENSIVE CARE BED

ApplicantEthos Medical Products , Ltd., Athlone, IE
DecisionSubstantially Equivalent, Nov 26, 1990
ReceivedNov 13, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K905113

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.