Product code FWF— General, Plastic Surgery

3DSCOPE

Classification name
Camera, Television, Endoscopic, Without Audio
Device class
Class 1
Regulation
21 CFR 878.4160
Advisory panel
General, Plastic Surgery
Total cleared
23
First cleared
Most recent

Market context for product code FWF

FDA has cleared 23 devices under product code FWF between 1984 and 2006, filed by 21 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 FWF

Recent clearances under product code FWF

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