IMX — Board, Lap, Wheelchair Class I
FDA product code IMX covers "Board, Lap, Wheelchair", a Class I medical device regulated under 21 CFR 890.3910. Submissions are reviewed by the Physical Medicine panel. At least 2 recent 510(k) clearances have been granted under this product code.
Classification Details
- Product Code
- IMX
- Device Class
- Class I
- Regulation Number
- 890.3910
- Submission Type
- Review Panel
- PM
- Medical Specialty
- Physical Medicine
- Implant
- No