510(k) K181730 ยท FMI Needle, Hypodermic, Single Lumen
BD Vacutainer Eclipse UltraFill Blood Collection Needle
| Applicant | Becton, Dickinson and Company, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Mar 1, 2019 |
| Received | Jun 29, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181730
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.