Product code CDO— Clinical Chemistry

URIC ACID

Classification name
Acid, Uric, Uricase (U.V.)
Device class
Class 1
Regulation
21 CFR 862.1775
Advisory panel
Clinical Chemistry
Total cleared
31
First cleared
Most recent

Market context for product code CDO

FDA has cleared 31 devices under product code CDO between 1976 and 2004, filed by 24 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

last 15 years

Top applicants under product code CDO

Recent clearances under product code CDO

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