DU PONT LINX HD-25 LASR IMAGER

DU PONT LINX HD-25 LASR IMAGER is an FDA 510(k)-cleared medical device (K923042) 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 November 8, 1992. Regulation: 8.