FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
System, Test, Tumor Marker, For Detection Of Bladder Cancer
PMA: P940035
·
Supplement: S014
·
Decision Feb 27, 2017
Classifications
1
FEI Numbers
4
Registration Numbers
4
Basic Information
- Device Name
- System, Test, Tumor Marker, For Detection Of Bladder Cancer
- Trade Name
- MATRITECH NMP22(TM) TEST KIT
- PMA Number
- P940035
- Supplement Number
- S014
- 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
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- February 27, 2017
- Date Received
- January 30, 2017
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
New vendor for the resin contained in the nitrocellulose membrane, and extend expiry of the antigen and purified antibodies used in the test.
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 |