IQO — Device, Prosthesis Alignment Class I
FDA product code IQO covers "Device, Prosthesis Alignment", a Class I medical device regulated under 21 CFR 890.3025. Submissions are reviewed by the Physical Medicine panel.
Classification Details
- Product Code
- IQO
- Device Class
- Class I
- Regulation Number
- 890.3025
- Submission Type
- Review Panel
- PM
- Medical Specialty
- Physical Medicine
- Implant
- No