510(k) K860789 ยท FIE Needle, Fistula
JMD AV FISTULA NEEDLE (MODIFICATION)
| Applicant | Jms Co., Ltd., Hiroshima, JP |
| Decision | Substantially Equivalent, Mar 18, 1986 |
| Received | Feb 26, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860789
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.