510(k) K921352 ยท FOS Catheter, Umbilical Artery
VYGON POLYURETHANE VENOUS/ARTERIAL XRO UMBIL. CATH
| Applicant | Vygon Corp., Elizabeth NJ, US |
| Decision | Substantially Equivalent, Oct 26, 1992 |
| Received | Mar 19, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921352
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.