510(k) K171734 ยท IYE Accelerator, Linear, Medical
HP PRO Positioning Device
| Applicant | Orfit Industries NV, Wijnegem, BE |
| Decision | Substantially Equivalent, Jul 25, 2017 |
| Received | Jun 12, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171734
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.