MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING

MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING is an FDA 510(k)-cleared medical device (K953477) manufactured by The DU Pont Co.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 6, 1995. Regulation: 8.