510(k) K071701 ยท IYE Accelerator, Linear, Medical
TRACKLEAF-10
| Applicant | Direx Systems Corp., Canton MA, US |
| Decision | Substantially Equivalent, Jul 23, 2007 |
| Received | Jun 21, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K071701
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.