510(k) K002938 ยท FMI Needle, Hypodermic, Single Lumen
B-D ULTRA-FINE III PEN NEEDLE; MODEL 31G X 3/16
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Nov 29, 2000 |
| Received | Sep 21, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002938
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.