510(k) K941823 ยท GXD Generator, Lesion, Radiofrequency
LEKSELL NEURO GENERATOR AND ACCESSORIES
| Applicant | Elekta Instruments, Inc., Atlanta GA, US |
| Decision | Substantially Equivalent, Mar 22, 1996 |
| Received | Apr 13, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941823
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.