510(k) K880332 ยท DQX Wire, Guide, Catheter
MEDRAD OPEN ENDED GUIDEWIRE
| Applicant | Medrad, Inc., Indianola PA, US |
| Decision | Substantially Equivalent, Jul 28, 1988 |
| Received | Jan 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880332
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.