510(k) K222852 ยท FMI Needle, Hypodermic, Single Lumen
Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle
| Applicant | Nipro Medical Corporation, Miami FL, US |
| Decision | Substantially Equivalent, May 25, 2023 |
| Received | Sep 21, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222852
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.