FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Test, Prostate Specific Antigen, Free, (Noncomplexed) To Distinguish Prostate Cancer From Benign Conditions
PMA: P950021
·
Supplement: S023
·
Decision Oct 27, 2020
Classifications
1
FEI Numbers
15
Registration Numbers
15
Basic Information
- Device Name
- Test, Prostate Specific Antigen, Free, (Noncomplexed) To Distinguish Prostate Cancer From Benign Conditions
- Trade Name
- ADVIA Centaur PSA Readypack Reagents
- PMA Number
- P950021
- Supplement Number
- S023
- Device Class
- FDA Class 3
- Product Code
- MTG
- Generic Name
- Test, prostate specific antigen, free, (noncomplexed) to distinguish prostate cancer from benign conditions
- Medical Specialty
- Unknown
- Advisory Committee
- Immunology
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- October 27, 2020
- Date Received
- September 29, 2020
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Implementation of medical decision pools for use in the control system.
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 |
|---|---|---|---|
| MTG | Test, Prostate Specific Antigen, Free, (Noncomplexed) To Distinguish Prostate Cancer From Benign Conditions | FDA class 3 | Unknown |