Product code JJP— Clinical Chemistry

CENTRIPREP 100

Classification name
Electrode, Ion Selective (Non-Specified)
Device class
Class 1
Regulation
21 CFR 862.2050
Advisory panel
Clinical Chemistry
Total cleared
3
First cleared
Most recent

Market context for product code JJP

FDA has cleared 3 devices under product code JJP between 1986 and 1990, filed by 3 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 JJP

Recent clearances under product code JJP

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