510(k) K910259 ยท DQO Catheter, Intravascular, Diagnostic
SCHNEIDER MAGNARAIL PROBING CATHETER
| Applicant | Schneider Intl., Ltd., Plymouth MN, US |
| Decision | Substantially Equivalent, Apr 18, 1991 |
| Received | Jan 22, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910259
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.