MKB — Device, Germicidal, Ultraviolet Class II
FDA product code MKB covers "Device, Germicidal, Ultraviolet", a Class II medical device regulated under 21 CFR 880.6500. Submissions are reviewed by the General Hospital panel.
Classification Details
- Product Code
- MKB
- Device Class
- Class II
- Regulation Number
- 880.6500
- Submission Type
- Review Panel
- HO
- Medical Specialty
- General Hospital
- Implant
- No