510(k) K963972 ยท FOS Catheter, Umbilical Artery
NEO-CARE DUAL LUMEN UMBILICAL CATHETER
| Applicant | Klein-Baker Medical, Inc., San Antonio TX, US |
| Decision | Substantially Equivalent, Dec 24, 1996 |
| Received | Oct 3, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963972
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.