510(k) K182274 ยท FMF Syringe, Piston
Orbit Subretinal Delivery System
| Applicant | Orbit Biomedical, Inc., Ambler PA, US |
| Decision | Unknown, Nov 20, 2018 |
| Received | Aug 22, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182274
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.