
Neuro-Diagnostic Assoc.
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MEDI-DX 7000 is an FDA 510(k)-cleared medical device (K964622) manufactured by Neuro-Diagnostic Assoc.. This device is classified under the Neurology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 30, 1997. Regulation: 8.

ADC
SKU DX606933

MDF
SKU DX683863

3M Littmann
SKU DX771242

Welch Allyn
SKU DX297280