DU PONT MV DARKROOM CASSETTE

DU PONT MV DARKROOM CASSETTE is an FDA 510(k)-cleared medical device (K931074) 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 June 7, 1993. Regulation: 8.