510(k) K211210 ยท FMF Syringe, Piston
Sterile Auto-Disable Syringes with/without Needle for Single Use
| Applicant | Azur Medical Company, Inc., Richmond VA, US |
| Decision | Substantially Equivalent, Jan 27, 2022 |
| Received | Apr 23, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211210
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.