
Olympus
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OLYMPUS IMAGEMANAGER SYSTEM is an FDA 510(k)-cleared medical device (K934889) manufactured by Olympus. This device is classified under the Radiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 27, 1994. Regulation: 8.

ADC
SKU DX606933

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Welch Allyn
SKU DX297280