510(k) K001033 ยท DQX Wire, Guide, Catheter
AGILITY STEERABLE GUIDEWIRE
| Applicant | Cordis Neurovascular, Inc., Miami Lake FL, US |
| Decision | Substantially Equivalent, Apr 14, 2000 |
| Received | Mar 31, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K001033
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.