Product code GRT— Microbiology

AGGLUTINOTEST-TUBERCULOSIS

Classification name
Antiserum, Fluorescent, Mycobacterium Tuberculosis
Device class
Class 1
Regulation
21 CFR 866.3370
Advisory panel
Microbiology
Total cleared
1
First cleared
Most recent

Market context for product code GRT

FDA has cleared 1 device under product code GRT, all in 1979, filed by 1 applicant company. 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.

Top applicants under product code GRT

Recent clearances under product code GRT

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