510(k) K000843 ยท FIE Needle, Fistula
MODIFICATION TO JMS APHERESIS NEEDLE
| Applicant | Jms Co., Ltd., Hiroshima, JP |
| Decision | Substantially Equivalent, Apr 10, 2000 |
| Received | Mar 15, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K000843
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.