DeviceClearance

Product code KNK— Clinical Chemistry

URIC ACID REAGENT

Classification name
Acid, Uric, Uricase (Colorimetric)
Device class
Class 1
Regulation
21 CFR 862.1775
Advisory panel
Clinical Chemistry
Total cleared
118
First cleared
Most recent

Market context for product code KNK

FDA has cleared 118 devices under product code KNK between 1977 and 2011, filed by 79 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 KNK

Recent clearances under product code KNK

1–100 of 118

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