Product code GRB— Microbiology

FIAX TEST KIT FOR MUMPS-G ANTIBODIES

Classification name: Antiserum, Cf, Mumps Virus
Device class: Class 1
Regulation: 21 CFR 866.3380
Advisory panel: Microbiology
Total cleared: 2
First cleared: 1987-09-18
Most recent: 1987-10-06

Market context for product code GRB

FDA has cleared 2 devices under product code GRB, all in 1987, filed by 2 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.

Top applicants under product code GRB

Whittaker Bioproducts, Inc.1 clearance
Sita, Inc.1 clearance

Recent clearances under product code GRB

K872733 — FIAX TEST KIT FOR MUMPS-G ANTIBODIESWhittaker Bioproducts, Inc.·1987-10-06
K872699 — MUMPS CF ANTIGEN AND CONTROL ANTIGENSita, Inc.·1987-09-18

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