510(k) K760780 ยท FMI Needle, Hypodermic, Single Lumen
DOUBLE-ENDED NEEDLE
| Applicant | Travenol Laboratories, S.A., Walker MI, US |
| Decision | Substantially Equivalent, Nov 16, 1976 |
| Received | Oct 5, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760780
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.