510(k) K840322 ยท FIQ Cannula, A-V Shunt
HEMOFILTRATION CATHETER HF-100
| Applicant | Vas-Cath of Canada , Ltd., Walker MI, US |
| Decision | Substantially Equivalent, Apr 24, 1984 |
| Received | Jan 25, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840322
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.