ClearanceBrief
510(k) K893801 ยท IOQ Bed, Flotation Therapy, Powered

M.F.S. LOW AIR LOSS PULSATING BED

ApplicantMedical Flotation Systems, Inc., Herndon VA, US
DecisionSubstantially Equivalent, Jul 25, 1989
ReceivedMay 22, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K893801

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.