510(k) K891293 ยท KPQ System, Simulation, Radiation Therapy
SLS SIMULATOR (MODELS SLS-9 AND SLS-14)
| Applicant | Philips Medical Systems North America, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Apr 20, 1989 |
| Received | Mar 10, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891293
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.