FDA PMA FDA Class 3 Approved 🇺🇸 United States

Test, Immunity, Cell Mediated, Mycobacterium Tuberculosis

PMA: P180047 · Supplement: S003 · Decision Jul 23, 2020
Classifications
1
FEI Numbers
4
Registration Numbers
4

Basic Information

Device Name
Test, Immunity, Cell Mediated, Mycobacterium Tuberculosis
Trade Name
LIAISON QuantiFERON TB Gold Plus
PMA Number
P180047
Supplement Number
S003
Device Class
FDA Class 3
Product Code
NCD
Generic Name
TEST, IMMUNITY, CELL MEDIATED, MYCOBACTERIUM TUBERCULOSIS
Medical Specialty
Unknown
Advisory Committee
Microbiology
Decision
Approved
Decision Code
APPR
Decision Date
July 23, 2020
Date Received
June 4, 2020
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval of change in the LIAISON QuantiFERON-TB Gold Plus assay protocol reagent dispensation sequence.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NCD Test, Immunity, Cell Mediated, Mycobacterium Tuberculosis