DeviceClearance

Product code LRP— General, Plastic Surgery

EYE TRAY

Classification name
Tray, Surgical
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Total cleared
22
First cleared
Most recent

Market context for product code LRP

FDA has cleared 22 devices under product code LRP between 1976 and 1996, filed by 20 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 LRP

Recent clearances under product code LRP

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