Product code GPS— Microbiology

Q-FEVER

Classification name
Antigen, Cf, Q Fever
Device class
Class 1
Regulation
21 CFR 866.3500
Advisory panel
Microbiology
Total cleared
1
First cleared
Most recent

Market context for product code GPS

FDA has cleared 1 device under product code GPS, all in 1985, 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 GPS

Recent clearances under product code GPS

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