Cerebral Assessment Systems, Inc.
COGNIVUE
SKU DEN130033UPC PKQ
In Stock
—
IIFDA 510(k) Cleared (DEN130033)
1
Free shipping on orders over $99 · 30-day returns
Healix Assistant
Ask me anything about our products
Quick questions
Powered by Healix AI · Talk to a human
Cerebral Assessment Systems, Inc.
Free shipping on orders over $99 · 30-day returns
COGNIVUE is an FDA 510(k)-cleared medical device (DEN130033) manufactured by Cerebral Assessment Systems, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 4, 2015. Regulation: 8.
