Atlas FDA

QUANTIFERON-TB GOLD TEST

FDA premarket approval P010033/S026 · decided 2014-12-10

Approval details

PMA number
P010033
Supplement
S026
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
QUANTIFERON-TB GOLD TEST
Generic name
TEST, IMMUNITY, CELL MEDIATED, MYCOBACTERIUM TUBERCULOSIS
Applicant
Qiagen
Date received
2014-11-10
Decision date
2014-12-10
Days to decision
30 days
Decision code
OK30
Product code
NCD
Advisory committee
Microbiology
Expedited review
No
Location
Germantown, MD
Statement
CHANGE TO THE MANUFACTURING PROCESS FOR BULK PEPTIDE SOLUTIONS.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
artus HSV-1/2 QS-RGQ MDx Kit (K142738)Qiagen2014-12-19