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FDA product code GXC

Device, Electroconvulsive Therapy

NeurologyClass 321 CFR 882.5940
Verified
US regulatory classifications
US Product Code (FDA)
GXC
View Product Code Classification
US Risk Class (FDA)
Class 3
US Regulation (CFR)
21 CFR 882.5940
View CFR Regulation
Medical specialty
Neurology
Device characteristics
GMP exempt
No
Implantable
No
Life-sustaining
No
Third party review
Not Eligible
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About this record

Device, Electroconvulsive Therapy 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.