Product code JJM— Clinical Chemistry

ADVANCED MICRO-OSMOMETER MODEL 3300

Classification name
Osmometer For Clinical Use
Device class
Class 1
Regulation
21 CFR 862.2730
Advisory panel
Clinical Chemistry
Total cleared
12
First cleared
Most recent

Market context for product code JJM

FDA has cleared 12 devices under product code JJM between 1979 and 1997, filed by 5 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 JJM

Recent clearances under product code JJM

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