FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Antigen(Complexed),Prostate Specific,(Cpsa)
PMA: P990055
·
Supplement: S013
·
Decision Aug 30, 2010
Classifications
1
FEI Numbers
3
Registration Numbers
3
Basic Information
- Device Name
- Antigen(Complexed),Prostate Specific,(Cpsa)
- Trade Name
- ADVIA CENTAUR CPSA ASSAY
- PMA Number
- P990055
- Supplement Number
- S013
- Device Class
- FDA Class 3
- Product Code
- NAF
- Generic Name
- ANTIGEN(COMPLEXED),PROSTATE SPECIFIC,(CPSA)
- Medical Specialty
- Unknown
- Advisory Committee
- Immunology
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- August 30, 2010
- Date Received
- August 6, 2010
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
IMPLEMENTATION OF AN AUTOMATED PROCESS FOR MAKING A COMPONENT THAT IS COMMON TO THE PSA AND CPSA ASSAYS.
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 |
|---|---|---|---|
| NAF | Antigen(Complexed),Prostate Specific,(Cpsa) | FDA class 3 | Unknown |