510(k) K915174 ยท FIE Needle, Fistula
JMS APHERESIS NEEDLE
| Applicant | Jms Co., Ltd., Hiroshima, JP |
| Decision | Substantially Equivalent, Mar 2, 1993 |
| Received | Nov 15, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915174
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.