510(k) K951738 ยท FOS Catheter, Umbilical Artery
ARGYLE NEO-SERT TRIPLE LUMEN UMBILICAL VESSEL CATHETER
| Applicant | Sherwood Medical Co., St. Louis MO, US |
| Decision | Substantially Equivalent, Sep 29, 1995 |
| Received | Apr 14, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951738
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 29, 2025 | Cardinal Health 200, LLC Catalog No. 8888160648; Umbilical Vessel Catheter 5 French triple lumen Open, Classified |
FOS | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.