FDA product code POP

Cranial Motion Measurement Device

Neurology·Class 2·21 CFR 882.1630
US regulatory classifications
US Product Code (FDA)
POP
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US Risk Class (FDA)
Class 2
US Regulation (CFR)
21 CFR 882.1630
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Medical specialty
Neurology
Device characteristics
GMP exempt
No
Implantable
No
Life-sustaining
No
Third party review
Eligible
Definition

A cranial motion measurement device is a prescription device that utilizes accelerometers to measure the motion or acceleration of the skull. These measurements are not to be used for diagnostic purposes.

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About this record

Cranial Motion Measurement Device is a medical device type in the Neurology specialty. This page includes real-world medical device registration data worldwide for this device type, with registrations from US FDA, Brazil ANVISA, and other global markets.

View regulatory classifications, recent 510(k) clearances, active device registrations, and similar products registered globally under this device category. Pure Global AI's free directory provides comprehensive worldwide registration intelligence across 7,000+ medical device types and 21 specialties.