ClearanceBrief
510(k) K823095 ยท IKZ Bed, Patient Rotation, Powered

KINETIC MOTION BED

ApplicantMotion Manufacturers, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 3, 1982
ReceivedOct 20, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823095

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.