510(k) K012886 ยท HAW Neurological Stereotaxic Instrument
CBYON SYSTEM WITH IMAGE ENHANCED FLUOROSCOPY MODULE
| Applicant | Cbyon, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Oct 9, 2001 |
| Received | Aug 28, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K012886
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.