COGNIVUE— 510(k) DEN130033
UnknownCerebral Assessment Systems, Inc.
FDA 510(k) clearance DEN130033 for COGNIVUE, Unknown on 2015-06-05. Applicant: Cerebral Assessment Systems, Inc..
Clearance details
- Applicant
- Cerebral Assessment Systems, Inc.
- Product code
- Code PKQ
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Pittsford, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.