510(k) K813001 ยท FPB Filter, Infusion Line
FIBRI-FILTER 20
| Applicant | Tri-Med, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Nov 6, 1981 |
| Received | Oct 26, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813001
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.