ClearanceBrief
510(k) K911199 ยท FIE Needle, Fistula

JMS AV FISTULA NEEDLES

ApplicantJms Co., Ltd., Hiroshima, JP
DecisionSubstantially Equivalent, Aug 28, 1991
ReceivedMar 6, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K911199

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.