510(k) K083597 ยท HAW Neurological Stereotaxic Instrument
SONOWAND INVITE
| Applicant | Sonowand AS, Ne MN, US |
| Decision | Substantially Equivalent, Sep 25, 2009 |
| Received | Dec 5, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083597
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.