ClearanceBrief
510(k) K943433 ยท IOQ Bed, Flotation Therapy, Powered

TOTAL CONTACT SEAT RIPPLE SYSTEM

ApplicantNumotech, Inc., Sun Valley CA, US
DecisionSubstantially Equivalent, Jul 31, 1995
ReceivedJul 15, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K943433

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.