ClearanceBrief
510(k) K830754 ยท DXT Injector And Syringe, Angiographic

BLOOD PRESSURE MONITORING KITS,WALRUS

ApplicantMedical Parameters, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 12, 1983
ReceivedMar 10, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830754

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.