
Gendex Corp.
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PROCESSOR, RADIOGRAPHIC-FILM, AUTOMATIC, DENTAL is an FDA 510(k)-cleared medical device (K945682) manufactured by Gendex Corp.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 8, 1995. Regulation: 8.

ADC
SKU DX606933

MDF
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3M Littmann
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Welch Allyn
SKU DX297280