510(k) K854773 ยท FIE Needle, Fistula
SUPERCATH A.V. FISTULA
| Applicant | Togo Medikit Co., Ltd., Chiyoda-Ku Tokyo101 Japan, JP |
| Decision | Substantially Equivalent, Apr 8, 1986 |
| Received | Nov 29, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854773
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.