510(k) K201234 ยท FMF Syringe, Piston
BD SoloShot Mini Syringe/ BD Auto Disable Syringe
| Applicant | Becton, Dickinson and Company, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Jul 15, 2020 |
| Received | May 7, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201234
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.