DeviceClearance

Product code FYF— General, Plastic Surgery

BOUFFANT CAP

Classification name
Cap, Surgical
Device class
Class 1
Regulation
21 CFR 878.4040
Advisory panel
General, Plastic Surgery
Total cleared
32
First cleared
Most recent

Market context for product code FYF

FDA has cleared 32 devices under product code FYF between 1976 and 1997, filed by 22 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 FYF

Recent clearances under product code FYF

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