510(k) K031999 ยท HAW Neurological Stereotaxic Instrument
ELEKTA LEKSELL STEREOTACTIC SYSTEM WITH MR POST KIT
| Applicant | Elekta Instrument AB, Stockholm, SE |
| Decision | Substantially Equivalent, Jul 25, 2003 |
| Received | Jun 27, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K031999
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.