FDA PMA
FDA Class 3
Approved
🇺🇸 United States
System, Test, Tumor Marker, For Detection Of Bladder Cancer
PMA: P940035
·
Supplement: S004
·
Decision May 20, 2008
Classifications
1
FEI Numbers
4
Registration Numbers
4
Basic Information
- Device Name
- System, Test, Tumor Marker, For Detection Of Bladder Cancer
- Trade Name
- NMP22 BLADDERCHEK TEST KIT
- PMA Number
- P940035
- Supplement Number
- S004
- Device Class
- FDA Class 3
- Product Code
- NAH
- Generic Name
- System, test, tumor marker, for detection of bladder cancer
- Medical Specialty
- Unknown
- Advisory Committee
- Immunology
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- May 20, 2008
- Date Received
- March 27, 2008
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR A MANUFACTURING SITE LOCATED AT BINAX, INC., SCARBOROUGH, MAINE.
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 |
|---|---|---|---|
| NAH | System, Test, Tumor Marker, For Detection Of Bladder Cancer | FDA class 3 | Unknown |