PHARMASEED, MODEL BT-125-1

PHARMASEED, MODEL BT-125-1 is an FDA 510(k)-cleared medical device (K992008) 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 December 22, 1999. Regulation: 8.