
Actus, Inc.
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DIGITAL RADIATION DETECTOR is an FDA 510(k)-cleared medical device (K771301) manufactured by Actus, Inc.. This device is classified under the Radiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 3, 1977. Regulation: 8.

ADC
SKU DX606933

MDF
SKU DX683863

3M Littmann
SKU DX771242

Welch Allyn
SKU DX297280