510(k) K973684 ยท HAW Neurological Stereotaxic Instrument
LEKSELL VIEWSCOPE, LEKSELL SURGISCOPE, LEKSELL FREEHAND
| Applicant | Elekta Instrument AB, San Diego CA, US |
| Decision | Substantially Equivalent, Mar 31, 1998 |
| Received | Sep 26, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973684
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.