510(k) K083083 ยท DYB Introducer, Catheter
AGILIS NXT STEERABLE INTRODUCER
| Applicant | St Jude Medical, Minnetonka MN, US |
| Decision | Substantially Equivalent, Nov 6, 2008 |
| Received | Oct 16, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083083
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.