510(k) K943522 ยท DQX Wire, Guide, Catheter
THE PROMPT GUIDWIRE
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Dec 19, 1994 |
| Received | Jul 18, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943522
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.