ClearanceBrief
510(k) K082212 ยท DXT Injector And Syringe, Angiographic

SYRINGE WITH HANDI-FIL

ApplicantMallinckrodt Inc., Liebel-Flarsheim Business, Cincinnati OH, US
DecisionSubstantially Equivalent, Jan 22, 2009
ReceivedAug 6, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K082212

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.