DeviceClearance

Product code LZB— General Hospital

ARTHREX FINGERSHIELD FINGER GUARD, MODEL AR-7199-XX

Classification name
Finger Cot
Device class
Class 1
Regulation
21 CFR 880.6250
Advisory panel
General Hospital
Total cleared
5
First cleared
Most recent

Market context for product code LZB

FDA has cleared 5 devices under product code LZB between 1990 and 2005, filed by 5 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 LZB

Recent clearances under product code LZB

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