510(k) K930982 ยท DQX Wire, Guide, Catheter
ILLUSION STEERABLE MICROGUIDEWIRE FOR NEUROVAC USE
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Feb 24, 1994 |
| Received | Feb 25, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930982
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.