510(k) K210464 ยท FMF Syringe, Piston
Auto Disable Syringe
| Applicant | Anhui Tiankang Medical Technology Co., Ltd., Tianchang, CN |
| Decision | Substantially Equivalent, Aug 24, 2021 |
| Received | Feb 16, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210464
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.