IMO — Handrim, Wheelchair Class I

FDA Device Classification

FDA product code IMO covers "Handrim, Wheelchair", a Class I medical device regulated under 21 CFR 890.3920. Submissions are reviewed by the Physical Medicine panel.

Classification Details

Product Code
IMO
Device Class
Class I
Regulation Number
890.3920
Submission Type
Review Panel
PM
Medical Specialty
Physical Medicine
Implant
No