DeviceClearance

Product code JRL— Clinical Chemistry

ACRO PACK

Classification name
Unit, Filter, Membrane
Device class
Class 1
Regulation
21 CFR 862.2050
Advisory panel
Clinical Chemistry
Total cleared
9
First cleared
Most recent

Market context for product code JRL

FDA has cleared 9 devices under product code JRL between 1978 and 1982, 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 JRL

Recent clearances under product code JRL

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