ClearanceBrief
510(k) K893708 ยท IOQ Bed, Flotation Therapy, Powered

FLUIDIZED AIR BED

ApplicantGsi Development Co., Carmel NY, US
DecisionSubstantially Equivalent, Jun 22, 1989
ReceivedMay 18, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K893708

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.