510(k) K991904 ยท FMI Needle, Hypodermic, Single Lumen
MODIFICATION OF JMS NEEDLES AND JMS SYRINGES
| Applicant | Jms Co., Ltd., Hiroshima, 730, JP |
| Decision | Substantially Equivalent, Aug 31, 1999 |
| Received | Jun 4, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991904
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.