FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Test, Immunity, Cell Mediated, Mycobacterium Tuberculosis
PMA: P010033
·
Supplement: S014
·
Decision Jan 29, 2010
Classifications
1
FEI Numbers
4
Registration Numbers
4
Basic Information
- Device Name
- Test, Immunity, Cell Mediated, Mycobacterium Tuberculosis
- Trade Name
- QUANTIFERON - TB GOLD AND TB GOLD IN-TUBE
- PMA Number
- P010033
- Supplement Number
- S014
- 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
- January 29, 2010
- Date Received
- June 2, 2009
- Supplement Type
- 135 Review Track For 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR THE USE OF THE DRY ROOM AT SCANTIBODIES LABORATORY, INC., SANTEE, CALIFORNIA, TO BE USED AS AN ALTERNATIVE METHOD TO VACUUM DRYING IN THE MANUFACTURING PROCESS OF ELISA PLATES.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| NCD | Test, Immunity, Cell Mediated, Mycobacterium Tuberculosis | FDA class 3 | Unknown |