GXC — Device, Electroconvulsive Therapy Class III

FDA Device Classification

FDA product code GXC covers "Device, Electroconvulsive Therapy", a Class III medical device regulated under 21 CFR 882.5940. Submissions are reviewed by the Neurology panel.

Classification Details

Product Code
GXC
Device Class
Class III
Regulation Number
882.5940
Submission Type
Review Panel
NE
Medical Specialty
Neurology
Implant
No