ClearanceBrief
510(k) K121521 ยท DYB Introducer, Catheter

AXERA ACCESS SYSTEM

ApplicantArstasis, Inc., Redwood City CA, US
DecisionSubstantially Equivalent, Jun 21, 2012
ReceivedMay 23, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K121521

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.