510(k) K914926 ยท KPQ System, Simulation, Radiation Therapy
SCANDIPLAN - VERSION 338
| Applicant | Scanditronix, Inc., Essex MA, US |
| Decision | Substantially Equivalent, May 28, 1992 |
| Received | Nov 4, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914926
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.