ClearanceBrief
510(k) K771206 ยท FIE Needle, Fistula

AV FISTULA NEEDLE SET

ApplicantTerumo America, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 15, 1977
ReceivedJul 5, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K771206

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.