Product code ILI— Physical Medicine

ARM SLING

Classification name
Sling, Arm
Device class
Class 1
Regulation
21 CFR 890.3640
Advisory panel
Physical Medicine
Total cleared
21
First cleared
Most recent

Market context for product code ILI

FDA has cleared 21 devices under product code ILI between 1976 and 1991, filed by 14 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 ILI

Recent clearances under product code ILI

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