Product code LRW— General, Plastic Surgery

69-120 TO 69-132 VARIOUS NAIL SCISSORS

Classification name
Scissors, General, Surgical
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Total cleared
18
First cleared
Most recent

Market context for product code LRW

FDA has cleared 18 devices under product code LRW between 1985 and 1991, filed by 11 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 LRW

Recent clearances under product code LRW

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