GE LOGIQ 700 DIAGNOSTIC ULTRASOUND SYSTEM

GE LOGIQ 700 DIAGNOSTIC ULTRASOUND SYSTEM is an FDA 510(k)-cleared medical device (K964617) 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 October 2, 1997. Regulation: 8.