510(k) K082304 ยท DQX Wire, Guide, Catheter
ROLL-X GUIDEWIRE
| Applicant | St Jude Medical, Minnetonka MN, US |
| Decision | Substantially Equivalent, Aug 27, 2008 |
| Received | Aug 13, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082304
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.