PHARMASEED, MODEL BT-103-1

PHARMASEED, MODEL BT-103-1 is an FDA 510(k)-cleared medical device (K992007) manufactured by Syncor Pharmaceuticals, 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 January 13, 2000. Regulation: 8.