
Wipro GE Healthcare Private, Ltd.
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GE VIVID P3 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM is an FDA 510(k)-cleared medical device (K102104) manufactured by Wipro GE Healthcare Private, Ltd.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 30, 2010. Regulation: 8.