QUANTIFERON-TB KIT
FDA premarket approval P010033/S005 · decided 2003-05-12
Approval details
- PMA number
- P010033
- Supplement
- S005
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- QUANTIFERON-TB KIT
- Generic name
- TEST, IMMUNITY, CELL MEDIATED, MYCOBACTERIUM TUBERCULOSIS
- Applicant
- Qiagen
- Date received
- 2003-04-18
- Decision date
- 2003-05-12
- Days to decision
- 24 days
- Decision code
- OK30
- Product code
- NCD
- Advisory committee
- Microbiology
- Expedited review
- No
- Location
- Germantown, MD
- Statement
- CHANGE THE SUPPLIER FOR PHYTOHAEMAGGLU-TININ (PHA-P), WHICH IS USED TO FORMULATE THE MITOGEN COMPONENT IN THE QUANTIFERON-TB KIT.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| artus HSV-1/2 QS-RGQ MDx Kit (K142738) | Qiagen | 2014-12-19 |