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Questions people ask
Is KBO cleared by the FDA?
No. KBO is an investigational device, not cleared by the FDA and not available for sale.
What does KBO measure?
EEG from sensors at the front and back of the head, and the brain's response to short tones played through earphones.
Does it replace the anesthesiologist's judgment?
No. It is designed to give the care team more information, not to make decisions for them.
How is it different from other depth monitors?
It is designed to read more of the brain rather than a single forehead index, and to compare each patient with their own pre-op baseline.
Where is KBO used in the patient journey?
Pre-op, during surgery and in recovery, as one continuous record.
Who is behind KBO?
KBO Systems, working with anesthesiologists at UC Davis. Meet the team.