DeviceClearance

Product code IQB— Physical Medicine

REAR FASTENING SAFETY STRAP

Classification name
Belt, Wheelchair
Device class
Class 1
Regulation
21 CFR 890.3920
Advisory panel
Physical Medicine
Total cleared
2
First cleared
Most recent

Market context for product code IQB

FDA has cleared 2 devices under product code IQB, all in 1978, filed by 1 applicant company. 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 IQB

Recent clearances under product code IQB

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