ClearanceBrief
510(k) K103143 ยท DYB Introducer, Catheter

ARSTASIS ONE LATCHWIRE ACCESS SYSTEM

ApplicantArstasis, Inc., San Carlos CA, US
DecisionSubstantially Equivalent, Feb 2, 2011
ReceivedOct 25, 2010
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K103143

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.