Product code DGQ— Immunology

ANTI-HUMAN SERUM

Classification name
Whole Blood Plasma, Antigen, Antiserum, Control
Device class
Class 1
Regulation
21 CFR 866.5700
Advisory panel
Immunology
Total cleared
1
First cleared
Most recent

Market context for product code DGQ

FDA has cleared 1 device under product code DGQ, 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 DGQ

Recent clearances under product code DGQ

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