510(k) K990510 ยท FIE Needle, Fistula
JMS APHERESIS NEEDLE
| Applicant | Jms Co., Ltd., Hiroshima, JP |
| Decision | Substantially Equivalent, Aug 30, 1999 |
| Received | Feb 18, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990510
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.