510(k) K945934 ยท DQX Wire, Guide, Catheter
URESIL(R) GUIDEWIRE
| Applicant | Uresil Corp., Skokie IL, US |
| Decision | Substantially Equivalent, Jul 10, 1995 |
| Received | Dec 5, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945934
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.