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 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
- 1994
- 1993
- 1986
- 1983
- 1982
- 1981
- 1980
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.