Product code FZS— General, Plastic Surgery

ACU-CURETTE

Classification name
Curette, Surgical, General Use
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Total cleared
14
First cleared
Most recent

Market context for product code FZS

FDA has cleared 14 devices under product code FZS between 1981 and 1994, filed by 13 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 FZS

Recent clearances under product code FZS

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