DeviceClearance

Product code ILG— Physical Medicine

ORTHOPEDIC STOCKINETTE

Classification name
Stocking, Elastic
Device class
Class 1
Regulation
21 CFR 890.3475
Advisory panel
Physical Medicine
Total cleared
8
First cleared
Most recent

Market context for product code ILG

FDA has cleared 8 devices under product code ILG between 1976 and 1983, filed by 8 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 ILG

Recent clearances under product code ILG

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