Product code ILP— Physical Medicine

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Classification name
System, Communication, Non-Powered
Device class
Class 1
Regulation
21 CFR 890.3700
Advisory panel
Physical Medicine
Total cleared
21
First cleared
Most recent

Market context for product code ILP

FDA has cleared 21 devices under product code ILP between 1976 and 1985, filed by 4 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 ILP

Recent clearances under product code ILP

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