510(k) K914863 ยท DQX Wire, Guide, Catheter
CORDIS CINCH(R) STEERABLE GUIDEWIRE EXT W/SLX COAT
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Dec 18, 1991 |
| Received | Oct 29, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914863
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.