510(k) K946033 ยท HAW Neurological Stereotaxic Instrument
LEIBINGER STEREOPLAN PLUS STEROTACTIC TREATMENT PLAN ING SOFTWARE PACKAGE
| Applicant | Leibinger GmbH, Washington DC, US |
| Decision | Substantially Equivalent, Sep 1, 1995 |
| Received | Dec 9, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K946033
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.