510(k) K970737 ยท FMI Needle, Hypodermic, Single Lumen
B-D ULTRA-FINE II SHORT 31G X 5/16 PEN NEEDLE
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Franklin Lake NJ, US |
| Decision | Substantially Equivalent, Mar 28, 1997 |
| Received | Feb 28, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970737
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.