Product code CCX— Anesthesiology

AIR UTERINE DISPLACER-AUD 120

Classification name
Support, Patient Position
Device class
Class 1
Regulation
21 CFR 868.6820
Advisory panel
Anesthesiology
Total cleared
8
First cleared
Most recent

Market context for product code CCX

FDA has cleared 8 devices under product code CCX between 1980 and 1994, filed by 8 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 CCX

Recent clearances under product code CCX

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