510(k) K200932 ยท FMI Needle, Hypodermic, Single Lumen
Blood Collection Needles
| Applicant | Vacutest Kima Srl, Arzegrande, IT |
| Decision | Substantially Equivalent, Dec 14, 2021 |
| Received | Apr 7, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200932
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.