510(k) K860241 ยท FIE Needle, Fistula
JMS AV FISTULA NEEDLE
| Applicant | Jms Co., Ltd., Hiroshima, JP |
| Decision | Substantially Equivalent, Feb 5, 1986 |
| Received | Jan 24, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860241
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.