510(k) K831801 ยท FIQ Cannula, A-V Shunt
HEMOCLAV VENOUS CATHETER
| Applicant | Exo, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jul 7, 1983 |
| Received | Jun 3, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831801
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.