ClearanceBrief
510(k) K801618 ยท FIE Needle, Fistula

ARGYLE A-V MEDI-WING HEMODIALYSIS SET

ApplicantSherwood Medical Co., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 13, 1980
ReceivedJul 15, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801618

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.