510(k) K200325 ยท FMF Syringe, Piston
Orbit Subretinal Delivery System
| Applicant | Orbit Biomedical, Ambler PA, US |
| Decision | Substantially Equivalent, Jul 14, 2020 |
| Received | Feb 10, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200325
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.