510(k) K960338 ยท IYE Accelerator, Linear, Medical
STEREOTACTIC BODY FRAME
| Applicant | Elekta Instrument AB, San Diego CA, US |
| Decision | Substantially Equivalent, Apr 23, 1996 |
| Received | Jan 24, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960338
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.