510(k) K974902 ยท FIE Needle, Fistula
JMS APHERESIS NEEDLE
| Applicant | Jms Co., Ltd., Hiroshima, JP |
| Decision | Substantially Equivalent, Mar 30, 1998 |
| Received | Dec 30, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974902
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.