510(k) K912156 ยท DQX Wire, Guide, Catheter
SCHNEIDER MAGNUM PERIPHERAL RECANAL GUIDEWIRE
| Applicant | Schneider Intl., Ltd., Plymouth MN, US |
| Decision | Substantially Equivalent, Sep 6, 1991 |
| Received | May 14, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912156
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.