510(k) K931019 ยท FMI Needle, Hypodermic, Single Lumen
BECTON DICKINSON LOCKING SAFETY-GARD(TM) IV NEEDLE
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Oct 18, 1993 |
| Received | Feb 26, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931019
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.