510(k) K924439 ยท FMI Needle, Hypodermic, Single Lumen
BECTON DICKINSON INTERLINK VIAL ACCESS CANNULA
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Feb 12, 1993 |
| Received | Sep 1, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924439
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.