510(k) K902422 ยท FMI Needle, Hypodermic, Single Lumen
NEEDLE, ASPIRATION & INJECTION, DISPOSABLE
| Applicant | Gainor Medical Europe, Ltd., Mcdonough GA, US |
| Decision | Substantially Equivalent, Jun 6, 1991 |
| Received | May 31, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902422
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.