510(k) K031200 ยท FMI Needle, Hypodermic, Single Lumen
MODIFICATION TO BD ULTRA-FINE III PEN NEEDLE
| Applicant | Becton, Dickinson & CO, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Jun 24, 2003 |
| Received | Apr 16, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K031200
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.