DU PONT COMPACT DAYLIGHT SYSTEM 2000

DU PONT COMPACT DAYLIGHT SYSTEM 2000 is an FDA 510(k)-cleared medical device (K922483) manufactured by E.I. Dupont DE Nemours & Co., 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 September 10, 1992. Regulation: 8.