ClearanceBrief
510(k) K802833 ยท IKY Mattress, Flotation Therapy, Non-Powered

TETRA NATAL-MAT WATER FLOTATION MAT.

ApplicantTetra Group U.S.A., Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 10, 1980
ReceivedNov 12, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802833

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.