ClearanceBrief
510(k) K002352 ยท FIE Needle, Fistula

JMS A.V. FISTULA NEEDLE SET ACCORDION TYPE

ApplicantJms Co., Ltd., Hiroshima, JP
DecisionSubstantially Equivalent, Sep 6, 2001
ReceivedAug 2, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K002352

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.