510(k) K981630 ยท FOS Catheter, Umbilical Artery
VYGON DOUBLE LUMEN UMBILICAL CATHETER
| Applicant | Schiff & Co., West Cadwell NJ, US |
| Decision | Substantially Equivalent, Oct 1, 1998 |
| Received | May 7, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981630
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.