
Ge Oec Medical Systems
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FLEXIVIEW 8800 DIGITAL MOBILE IMAGING SYSTEM is an FDA 510(k)-cleared medical device (K003837) manufactured by Ge Oec 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 March 11, 2001. Regulation: 8.