510(k) K223286 · FMI Needle, Hypodermic, Single Lumen
BD AutoShield Duo Pen Needle
| Applicant | Becton, Dickinson and Company, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Dec 28, 2022 |
| Received | Oct 25, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223286
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.