Argus Cognitive, Inc.
Argus Cognitive ReVISION Software
SKU K223322UPC LLZ
In Stock
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IIFDA 510(k) Cleared (K223322)
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Free shipping on orders over $99 · 30-day returns
Argus Cognitive, Inc.
Free shipping on orders over $99 · 30-day returns
Argus Cognitive ReVISION Software is an FDA 510(k)-cleared medical device (K223322) manufactured by Argus Cognitive, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 23, 2023. Regulation: 8.
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