510(k) K790086 ยท FMI Needle, Hypodermic, Single Lumen
NEEDLE, TRUCARE VACUTAINER
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Washington DC, US |
| Decision | Substantially Equivalent, Feb 8, 1979 |
| Received | Jan 17, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790086
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.