FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Total, Prostate Specific Antigen (Noncomplexed & Complexed) For Detection Of Prostate Cancer
PMA: P850048
·
Supplement: S043
·
Decision Nov 9, 2016
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
- TANDEM-R PSA IMMUNORADIOMETRIC ASSAY
- PMA Number
- P850048
- Supplement Number
- S043
- 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
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- November 9, 2016
- Date Received
- October 11, 2016
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Change in the manufacturing process for the conversion from a Hollow Fiber particle coupling process to a Semi-Automated Magnetic separation particle coupling process used for the paramagnetic particles in the Access Hybritech PSA.
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 |