GRBClass I

Antiserum, Cf, Mumps Virus

21 CFR 866.3380 / Microbiology

GRB is the FDA product code for Antiserum, Cf, Mumps Virus, a class I device type, regulated under 21 CFR 866.3380. As of 2026-09-10, FDA records hold 2 510(k) clearances under this code, the most recent dated 1987-10-06, and no recalls.

Classification record

Product code: GRB
Device name: Antiserum, Cf, Mumps Virus
Regulation: 21 CFR 866.3380
Device class: Class I
Review panel: Microbiology
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 2
Ingested recalls: 0

Clearances, product code GRB

By decision year

2 clearances under product code GRB with a decision year between 1987 and 1987, 1987 the highest year at 2.

Show the numbers

510(k) clearances under FDA product code GRB by decision year
Year	Clearances
1987	2

Applicants with the most clearances

Product code GRB

Applicants holding the most 510(k) clearances under product code GRB
Applicant	Clearances
Sita, Inc.	1
Whittaker Bioproducts, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code GRB.

Recent clearances

Product code GRB

Recent recalls

Product code GRB

FDA records show no recalls under product code GRB.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)