510(k) K941814 ยท FOS Catheter, Umbilical Artery
ARGYLE DUAL LUMEN UMBILICAL VESSEL CATHETER
| Applicant | Sherwood Medical Co., St. Louis MO, US |
| Decision | Substantially Equivalent, Sep 30, 1994 |
| Received | Apr 12, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941814
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 29, 2025 | Cardinal Health 200, LLC Catalog No. 8888160556; Umbilical Vessel Catheter 5 French dual 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.