510(k) K831440 ยท FIQ Cannula, A-V Shunt
SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260
| Applicant | Med-West, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jun 3, 1983 |
| Received | May 5, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831440
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.