1989 SOFTWARE REVISION TO THE BMT-1100

1989 SOFTWARE REVISION TO THE BMT-1100 is an FDA 510(k)-cleared medical device (K894714) manufactured by Bruker Medical Imaging, 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 14, 1989. Regulation: 8.