ClearanceBrief
510(k) K962788 ยท IKZ Bed, Patient Rotation, Powered

CLINIDYNE ROTATIONAL THERAPY MATTRESS SYSTEM

ApplicantGaymar Industries, Inc., Orchard Park NY, US
DecisionSubstantially Equivalent, Apr 30, 1997
ReceivedJul 17, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K962788

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.