FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Total, Prostate Specific Antigen (Noncomplexed & Complexed) For Detection Of Prostate Cancer
PMA: P000021
·
Supplement: S018
·
Decision Mar 11, 2011
Classifications
1
FEI Numbers
15
Registration Numbers
15
Basic Information
- Device Name
- Total, Prostate Specific Antigen (Noncomplexed & Complexed) For Detection Of Prostate Cancer
- Trade Name
- DIMENSION FPSA FLEX REAGENT CARTRIDGE
- PMA Number
- P000021
- Supplement Number
- S018
- Device Class
- FDA Class 3
- Product Code
- MTF
- Generic Name
- Total, prostate specific antigen (noncomplexed & complexed) for detection of prostate cancer
- Medical Specialty
- Unknown
- Advisory Committee
- Immunology
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- March 11, 2011
- Date Received
- August 19, 2010
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR SOFTWARE CHANGES (VERSION 3.1.1. TO 3.3.) AND ASSOCIATED HARDWARE CHANGES TO THE DIMENSION VISTA 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 |
|---|---|---|---|
| MTF | Total, Prostate Specific Antigen (Noncomplexed & Complexed) For Detection Of Prostate Cancer | FDA class 3 | Unknown |