GENERAL ELECTRIC AMX 110, AMX II AND AMX 3

GENERAL ELECTRIC AMX 110, AMX II AND AMX 3 is an FDA 510(k)-cleared medical device (K944442) manufactured by Pro-Tronics, 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 March 13, 1995. Regulation: 8.