FDA product code JXK
Cranial Electrotherapy Stimulator To Treat Depression
Neurology·Class 3·21 CFR 882.5800
US regulatory classifications
- US Product Code (FDA)
- JXKView Product Code Classification →
- US Risk Class (FDA)
- Class 3
- US Regulation (CFR)
- 21 CFR 882.5800View 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
Cranial Electrotherapy Stimulator To Treat Depression 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.