
Neuronetics, Inc.
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NeuroStar TMS Therapy System is an FDA 510(k)-cleared medical device (K160703) manufactured by Neuronetics, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 9, 2016. Regulation: 8.

ADC
SKU DX606933

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3M Littmann
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Welch Allyn
SKU DX297280