FDA PMA FDA Class 3 Approved 🇺🇸 United States

Test, Prostate Specific Antigen, Free, (Noncomplexed) To Distinguish Prostate Cancer From Benign Conditions

PMA: P020027 · Supplement: S012 · Decision Sep 2, 2010
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
DIMENSIONS FPSA FLEX REAGENT CARTRIDGE
PMA Number
P020027
Supplement Number
S012
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
Approved
Decision Code
APPR
Decision Date
September 2, 2010
Date Received
July 6, 2010
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR THE ADDITION OF A CLOT CHECK DEVICE TO THE DIMENSION EXL WITH LM SYSTEM WHEN USED WITH THE DIMENSION FPSA FLEX REAGENT CARTRIDGE.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MTG Test, Prostate Specific Antigen, Free, (Noncomplexed) To Distinguish Prostate Cancer From Benign Conditions