GWR — Generator, Electroencephalograph Test Signal Class I
FDA product code GWR covers "Generator, Electroencephalograph Test Signal", a Class I medical device regulated under 21 CFR 882.1430. Submissions are reviewed by the Neurology panel.
Classification Details
- Product Code
- GWR
- Device Class
- Class I
- Regulation Number
- 882.1430
- Submission Type
- Review Panel
- NE
- Medical Specialty
- Neurology
- Implant
- No