510(k) K010472 ยท IYE Accelerator, Linear, Medical
PATIENT DOSE VERIFICATION SYSTEM, MODEL TN-RD-50
| Applicant | Thomson & Nielsen Electronics, Ltd., Ottawa, Ontario, CA |
| Decision | Substantially Equivalent, May 8, 2001 |
| Received | Feb 20, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010472
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.