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COGNIVUE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN130033
510(k) Type
Direct
Applicant
CEREBRAL ASSESSMENT SYSTEMS, INC
Country
United States
FDA Decision
Deleted
Decision Date
6/5/2015
Days to Decision
723 days

COGNIVUE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN130033
510(k) Type
Direct
Applicant
CEREBRAL ASSESSMENT SYSTEMS, INC
Country
United States
FDA Decision
Deleted
Decision Date
6/5/2015
Days to Decision
723 days