DeviceClearance

Product code IMX— Physical Medicine

LAP BOARD W/RIM

Classification name
Board, Lap, Wheelchair
Device class
Class 1
Regulation
21 CFR 890.3910
Advisory panel
Physical Medicine
Total cleared
2
First cleared
Most recent

Market context for product code IMX

FDA has cleared 2 devices under product code IMX, all in 1978, filed by 2 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Top applicants under product code IMX

Recent clearances under product code IMX

Data sourced from openFDA. This site is unofficial and independent of the FDA.