FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Somatic Gene Mutation Detection System
PMA: P120014
·
Supplement: S004
·
Decision Apr 1, 2015
Classifications
1
FEI Numbers
11
Registration Numbers
11
Basic Information
- Device Name
- Somatic Gene Mutation Detection System
- Trade Name
- THXID BRAF KIT
- PMA Number
- P120014
- Supplement Number
- S004
- Device Class
- FDA Class 3
- Product Code
- OWD
- Generic Name
- Somatic gene mutation detection system
- Medical Specialty
- Unknown
- Advisory Committee
- Pathology
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- April 1, 2015
- Date Received
- March 3, 2015
- Supplement Type
- Special (Immediate Track)
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR ADDITION OF A QUALITY CONTROL TEST FOR THE THXID¿-BRAF MASTERMIX.
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 |
|---|---|---|---|
| OWD | Somatic Gene Mutation Detection System | FDA class 3 | Unknown |