510(k) K962765 ยท DQX Wire, Guide, Catheter
CORDIS MARKER WIRE STEERABLE GUIDEWIRE (STABILIZER WITH RADIOPAQUE MARKERS) AND (WIZDOM WITH RADIOPAQUE MARKERS)
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Feb 21, 1997 |
| Received | Jul 16, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962765
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.