
Ajex Meditech., Ltd.
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AJEX 1200 H / AJEX 240H MOBILE X-RAY GENERATOR is an FDA 510(k)-cleared medical device (K122298) manufactured by Ajex Meditech., 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 March 27, 2014. Regulation: 8.