510(k) K911612 ยท IYE Accelerator, Linear, Medical
NUCLETRON PLANNING SYSTEM
| Applicant | Nucletron-Oldelft Corp., Columbia MD, US |
| Decision | Substantially Equivalent, Jun 13, 1991 |
| Received | Apr 11, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911612
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.