510(k) K031980 ยท HAW Neurological Stereotaxic Instrument
MODIFICATION TO LEKSELL STEREOTACTIC SYSTEM
| Applicant | Elekta Instrument AB, Stockholm, SE |
| Decision | Substantially Equivalent, Jul 25, 2003 |
| Received | Jun 26, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K031980
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.