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Medical Devices; Neurological Devices; Classification of Cranial Motion Measurement Device. Final order.

出版信息

Fed Regist. 2017 Jul 28;82(144):35069-71.

Abstract

The Food and Drug Administration (FDA or Agency) is classifying the cranial motion measurement device into class II (special controls). The special controls that will apply to the device are identified in this order and will be part of the codified language for the cranial motion measurement device’s classification. The Agency is classifying the device into class II (special controls) in order to provide a reasonable assurance of safety and effectiveness of the device.

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