510(k) K890207 ยท DQX Wire, Guide, Catheter
INTERVENTIONAL PRODUCTS - GUIDE WIRES
| Applicant | E-Z-Em, Inc., Marlboro NJ, US |
| Decision | Substantially Equivalent, May 31, 1989 |
| Received | Jan 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890207
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.