FDA PMA FDA Class 3 Approved 🇺🇸 United States

System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection

PMA: P130017 · Supplement: S010 · Decision Aug 19, 2016
Classifications
1
FEI Numbers
11
Registration Numbers
11

Basic Information

Device Name
System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection
Trade Name
COLOGUARD
PMA Number
P130017
Supplement Number
S010
Device Class
FDA Class 3
Product Code
PHP
Generic Name
System, colorectal neoplasia, DNA methylation and hemoglobin detection
Medical Specialty
Unknown
Advisory Committee
Pathology
Decision
Approved
Decision Code
APPR
Decision Date
August 19, 2016
Date Received
May 31, 2016
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for design changes to Cologuard Collection Kit and associated patient labeling.

Classifications

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

Product Code Device Name
PHP System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection