PathAI, Inc.
AISight Dx
SKU K243391UPC QKQ
In Stock
—
IIFDA 510(k) Cleared (K243391)
1
Free shipping on orders over $99 · 30-day returns
PathAI, Inc.
Free shipping on orders over $99 · 30-day returns
AISight Dx is an FDA 510(k)-cleared medical device (K243391) manufactured by PathAI, Inc.. This device is classified under the Pathology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 25, 2025. Regulation: 8.
