510(k) K970962 ยท FIE Needle, Fistula
JMS AV FISTULA NEEDLE
| Applicant | Jms Co., Ltd., Hiroshima, 730, JP |
| Decision | Substantially Equivalent, Aug 7, 1997 |
| Received | Mar 17, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970962
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.