Product code CDG— Clinical Chemistry
URINARY 17-KETOSTERIOD/17
- Classification name
- Chromatography Separation/Zimmerman 17-Ketogenic Steroids
- Device class
- Class 1
- Regulation
- 21 CFR 862.1385
- Advisory panel
- Clinical Chemistry
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code CDG
FDA has cleared device under product code CDG, all in 1978, filed by 1 applicant company. 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.
Top applicants under product code CDG
Recent clearances under product code CDG
Data sourced from openFDA. This site is unofficial and independent of the FDA.