510(k) K840339 ยท FOS Catheter, Umbilical Artery
UMBILICAL VESSEL CATHETER
| Applicant | Catheter Technology Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 25, 1984 |
| Received | Jan 25, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840339
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.