
Howtek, Inc.
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DIGITIZER DIRECTOR (HSC025-01) is an FDA 510(k)-cleared medical device (K972191) manufactured by Howtek, Inc.. This device is classified under the Radiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 7, 1997. Regulation: 8.

ADC
SKU DX606933

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3M Littmann
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Welch Allyn
SKU DX297280