510(k) K201816 ยท FMF Syringe, Piston
ARTHROTAP
| Applicant | Accuro Technologies, Inc., Victoria, CA |
| Decision | Substantially Equivalent, Oct 16, 2020 |
| Received | Jul 1, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201816
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.