510(k) K171350 ยท IYE Accelerator, Linear, Medical
Collision Check
| Applicant | Radformation, Inc., New York NY, US |
| Decision | Substantially Equivalent, Nov 29, 2017 |
| Received | May 9, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171350
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.