ClearanceBrief
510(k) K831401 ยท FIQ Cannula, A-V Shunt

SINGLE NEEDLE SUBCLAVIAN VEIN ACCESS

ApplicantMed-West, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 3, 1983
ReceivedMay 2, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K831401

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.