FDA PMA
FDA Class 2
Approved
🇺🇸 United States
Fluorescence Polarization Immunoassay For Cyclosporine
PMA: P890025
·
Supplement: S002
·
Decision Oct 4, 1990
Classifications
1
FEI Numbers
0
Registration Numbers
0
Basic Information
- Device Name
- Fluorescence Polarization Immunoassay For Cyclosporine
- Trade Name
- TDX CYCLOSPORINE AND METABOLITES WHOLE BLOOD ASSAY
- PMA Number
- P890025
- Supplement Number
- S002
- Device Class
- FDA Class 2
- Product Code
- MGU
- Generic Name
- Fluorescence polarization immunoassay for cyclosporine
- Regulation Number
- 862.1235
- Medical Specialty
- Clinical Chemistry
- Advisory Committee
- Clinical Toxicology
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- October 4, 1990
- Date Received
- April 2, 1990
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
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 |
|---|---|---|---|
| MGU | Fluorescence Polarization Immunoassay For Cyclosporine | FDA class 2 | Clinical Chemistry |