510(k) K964654 ยท FMI Needle, Hypodermic, Single Lumen
BECTON DICKINSON BLUNT PLASTIC CANNULA
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Apr 2, 1997 |
| Received | Nov 20, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964654
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.