PHARMASEED, MODEL BT-103-2

PHARMASEED, MODEL BT-103-2 is an FDA 510(k)-cleared medical device (K993700) manufactured by Syncor International, 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 1, 2000. Regulation: 8.