
Dept. of the Army
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HAND HELD DENTAL X-RAY DEVICE is an FDA 510(k)-cleared medical device (K934818) manufactured by Dept. of the Army. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 23, 1994. Regulation: 8.

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