IMM — Footrest, Wheelchair Class I

FDA Device Classification

FDA product code IMM covers "Footrest, Wheelchair", a Class I medical device regulated under 21 CFR 890.3920. 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
IMM
Device Class
Class I
Regulation Number
890.3920
Submission Type
Review Panel
PM
Medical Specialty
Physical Medicine
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K892791union industrial coPATIENT EXAMINATION GLOVES (LATEX)August 24, 1989
K821634fred sammonsEZ STAND MOBILE STOOLJune 11, 1982