ClearanceBrief
510(k) K853141 ยท KHE Reagent, Occult Blood

ACCESS DIGIWIPE SYSTEM

ApplicantMedtech Products, Inc., Miami FL, US
DecisionSubstantially Equivalent, Nov 18, 1985
ReceivedJul 24, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K853141

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.