510(k) K924591 ยท DQY Catheter, Percutaneous
SCHNEIDER SOLID-7 SOPTIP GUIDING CATHETER
| Applicant | Schneider Intl., Ltd., Plymouth MN, US |
| Decision | Substantially Equivalent, Dec 8, 1992 |
| Received | Sep 10, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924591
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.