510(k) K010511 ยท DQX Wire, Guide, Catheter
MODIFICATION TO: AGILITY STEERABLE GUIDEWIRES
| Applicant | Cordis Neurovascular, Inc., Miami Lake FL, US |
| Decision | Substantially Equivalent, Mar 1, 2001 |
| Received | Feb 21, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K010511
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.