510(k) K051746 ยท HAW Neurological Stereotaxic Instrument
ELEKTA ESARTE FRAME SYSTEM
| Applicant | Elekta Instrument AB, Stockholm, SE |
| Decision | Substantially Equivalent, Jul 25, 2005 |
| Received | Jun 29, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K051746
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.