ClearanceBrief
510(k) K990470 ยท FIE Needle, Fistula

JMS A. V. FISTULA NEEDLE SET

ApplicantJms Co., Ltd., Hiroshima, JP
DecisionSubstantially Equivalent, Aug 30, 1999
ReceivedFeb 16, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K990470

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.