ClearanceBrief
510(k) K090849 ยท DQY Catheter, Percutaneous

MODIFICATION TO: NANOCROSS 0.14 OTW PTA DILATATION CATHETER, MODELS AB14W020210090, AB14W020210150

ApplicantEv3, Inc., Plymouth MN, US
DecisionSubstantially Equivalent, May 1, 2009
ReceivedMar 30, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K090849

DateFirm and productCodeLinked 510(k)
Dec 23, 2010Ev3, Inc.
ev3 NanoCross 0.14 OTW PTA Dilatation Catheter, sterilized using ethylene oxide gas. REF #'s: AB14W040040150, AB14W030040150, AB14W020040150, AB14W025080150, AB14W020080150, AB14W020120150, AB14W030
Terminated
DQYNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.