IMX — Board, Lap, Wheelchair Class I

FDA Device Classification

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

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K780184orthopedic equipment coWHEELCHAIR ACCESSORIESFebruary 13, 1978
K772401fred sammonsLAP BOARD W/RIMJanuary 5, 1978