510(k) K931577 ยท DQX Wire, Guide, Catheter
SCHNEIDER MAGNUM PERIPHERAL RECANALIZATION GUIDEWI
| Applicant | Schneider Intl., Ltd., Plymouth MN, US |
| Decision | Substantially Equivalent, Jun 23, 1993 |
| Received | Mar 30, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931577
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.