FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

Test, Immunity, Cell Mediated, Mycobacterium Tuberculosis

PMA: P010033 · Supplement: S052 · Decision Jan 23, 2026
Classifications
1
FEI Numbers
0
Registration Numbers
0

Research PMA P010033 in seconds

The Research Assistant summarizes PMA approval history, supplements and related safety signals — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Test, Immunity, Cell Mediated, Mycobacterium Tuberculosis
Trade Name
QuantiFERON®-TB Gold Test and QuantiFERON®-TB Gold Plus Test
PMA Number
P010033
Supplement Number
S052
Device Class
FDA Class 3
Product Code
NCD
Generic Name
TEST, IMMUNITY, CELL MEDIATED, MYCOBACTERIUM TUBERCULOSIS
Medical Specialty
Unknown
Advisory Committee
Microbiology
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
January 23, 2026
Date Received
December 30, 2025
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

an internal site to internal site transfer of a manufacturing process

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