510(k) K103083 ยท DYB Introducer, Catheter
AGILIS ES STEERABLE INTRODUCER
| Applicant | St Jude Medical, Minnetonka MN, US |
| Decision | Substantially Equivalent, Apr 8, 2011 |
| Received | Oct 19, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103083
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.