510(k) K896041 ยท FOS Catheter, Umbilical Artery
GESCO DUAL LUMEN UMBILICATH II-DL
| Applicant | Gesco Intl., Inc., San Antonio TX, US |
| Decision | Unknown, Apr 17, 1990 |
| Received | Oct 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896041
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.