510(k) K895442 ยท KPQ System, Simulation, Radiation Therapy
THE X-RAY DIGITIZER, ALTEK MODEL ACT20020-BL
| Applicant | Altek Corp., Silver Spring MD, US |
| Decision | Substantially Equivalent, Dec 14, 1989 |
| Received | Sep 8, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895442
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.