
Omega Medical Imaging, LLC
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Nyquist.IQ is an FDA 510(k)-cleared medical device (K212890) manufactured by Omega Medical Imaging, LLC. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 12, 2021. Regulation: 8.

ADC
SKU DX606933

MDF
SKU DX683863

3M Littmann
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Welch Allyn
SKU DX297280