ClearanceBrief
510(k) K903659 ยท IOQ Bed, Flotation Therapy, Powered

STAGE III

ApplicantUnique Flotation Systems, Inc., Corona CA, US
DecisionSubstantially Equivalent, Sep 17, 1990
ReceivedAug 9, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K903659

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.