OR340 INTRAOPERATIVE ULTRASOUND BIOPSY NEEDLE GUID

OR340 INTRAOPERATIVE ULTRASOUND BIOPSY NEEDLE GUID is an FDA 510(k)-cleared medical device (K913987) manufactured by Codman & Shurtleff, Inc.. This device is classified under the Radiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 12, 1992. Regulation: 8.