510(k) K961639 ยท HAW Neurological Stereotaxic Instrument
LEKSELL IMAGE GUIDANCE SURGICAL SYSTEM (LIGS)
| Applicant | Elekta Instrument AB, Stockholm, SE |
| Decision | Substantially Equivalent, Jul 26, 1996 |
| Received | Apr 29, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961639
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.