LOGIQ A200 DIAGNOSTIC ULTRASOUND SYSTEM

LOGIQ A200 DIAGNOSTIC ULTRASOUND SYSTEM is an FDA 510(k)-cleared medical device (K960700) manufactured by GE Medical Systems. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 27, 1996. Regulation: 8.