JXK — Cranial Electrotherapy Stimulator To Treat Depression Class III
FDA product code JXK covers "Cranial Electrotherapy Stimulator To Treat Depression", a Class III medical device regulated under 21 CFR 882.5800. Submissions are reviewed by the Neurology panel.
Classification Details
- Product Code
- JXK
- Device Class
- Class III
- Regulation Number
- 882.5800
- Submission Type
- Review Panel
- NE
- Medical Specialty
- Neurology
- Implant
- No