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
MGU Fluorescence Polarization Immunoassay For Cyclosporine