Eastman Kodak Company
MODIFICATION TO KODAK DIRECTVIEW CR 800/900 SYSTEM
SKU K021829UPC MQB
In Stock
—
IIFDA 510(k) Cleared (K021829)
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
Eastman Kodak Company
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO KODAK DIRECTVIEW CR 800/900 SYSTEM is an FDA 510(k)-cleared medical device (K021829) manufactured by Eastman Kodak Company. 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 1, 2002. Regulation: 8.
