ClearanceBrief
510(k) K810220 ยท IKZ Bed, Patient Rotation, Powered

POWERED PATIENT SYSTEM

ApplicantTri W-G, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 4, 1981
ReceivedJan 27, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810220

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.