510(k) K896450 ยท GXD Generator, Lesion, Radiofrequency
NEURO N 50 LESION GENERATOR
| Applicant | Leibinger & Fischer , Ltd., Dallas TX, US |
| Decision | Substantially Equivalent, Mar 19, 1991 |
| Received | Nov 9, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896450
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.