ClearanceBrief
510(k) K083422 ยท DQY Catheter, Percutaneous

6F TAIGA GUIDING CATHETER

ApplicantMedtronic Vascular, Danvers MA, US
DecisionSubstantially Equivalent, Feb 6, 2009
ReceivedNov 19, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K083422

DateFirm and productCodeLinked 510(k)
Mar 29, 2018Medtronic Inc
6F Taiga Guiding Catheter
Terminated
DQYNone listed

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