ClearanceBrief
510(k) K133189 ยท DXT Injector And Syringe, Angiographic

DUAL SHOT ALPHA 7

ApplicantNemoto Kyorindo Co., Ltd., Bunkyo-Ku, JP
DecisionSubstantially Equivalent, Jun 30, 2014
ReceivedOct 17, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K133189

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.