510(k) K991636 ยท HAW Neurological Stereotaxic Instrument
ELEKTA STEREOTACTIC GUIDE
| Applicant | Elekta Instrument AB, Lake Forest CA, US |
| Decision | Substantially Equivalent, Jul 20, 1999 |
| Received | May 12, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991636
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.