510(k) K940660 ยท IYE Accelerator, Linear, Medical
MODEL 37-720 DUAL DIODE DOSIMETRY SYSTEM
| Applicant | Victoreen, Inc., Cleveland OH, US |
| Decision | Substantially Equivalent, Dec 9, 1994 |
| Received | Feb 15, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940660
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.