Product code KNO— Physical Medicine

WHEELCHAIR ACCESSORIES

Classification name
Accessories, Wheelchair
Device class
Class 1
Regulation
21 CFR 890.3910
Advisory panel
Physical Medicine
Total cleared
35
First cleared
Most recent

Market context for product code KNO

FDA has cleared 35 devices under product code KNO between 1976 and 1987, filed by 7 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.

Clearances per year

Top applicants under product code KNO

Recent clearances under product code KNO

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