FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

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

PMA: P020027 · Supplement: S021 · Decision Sep 25, 2014
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
DIMENSION VISTA FPSA FLEX REAGENT CARTRIDGE
PMA Number
P020027
Supplement Number
S021
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
30-Day Notice Accepted
Decision Code
OK30
Decision Date
September 25, 2014
Date Received
August 27, 2014
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

ADDITION OF AN ALTERNATE AUTOMATED COLUMN (INTERCHIM PURIFLASH® PURIFICATION SYSTEM) PURIFICATION PROCEDURE TO THE EXISTING MANUAL COLUMN CHROMATOGRAPHY PURIFICATION PROCEDURE IN THE EUROPIUM PARTICLE RAW MATERIAL (EPRM) MANUFACTURING PROCESS.

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