DU PONT LINX LASER IMAGER W/THE LINX NETWORKING

DU PONT LINX LASER IMAGER W/THE LINX NETWORKING is an FDA 510(k)-cleared medical device (K900935) manufactured by E.I. Dupont DE Nemours & Co., Inc.. This device is classified under the Radiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 14, 1990. Regulation: 8.