Product code LRJ— General Hospital

LONZA FORMULATION R-82

Classification name
Disinfectant, Medical Devices
Device class
Class 1
Regulation
21 CFR 880.6890
Advisory panel
General Hospital
Total cleared
73
First cleared
Most recent

Market context for product code LRJ

FDA has cleared 73 devices under product code LRJ between 1987 and 1999, filed by 34 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 LRJ

Adverse events under product code LRJ

product code LRJ
Injury
958
Total
958

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code LRJ

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