510(k) K100209 ยท FMI Needle, Hypodermic, Single Lumen
BD ECLIPSE NEEDLE WITH SMARTSLIP TECHNOLOGY
| Applicant | Becton, Dickinson & CO, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Feb 19, 2010 |
| Received | Jan 25, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K100209
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.