FDA PMA FDA Class 3 Approved 🇺🇸 United States

System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection

PMA: P130017 · Supplement: S057 · Decision Jul 20, 2024
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
S057
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
July 20, 2024
Date Received
January 26, 2024
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Labeling Change - PAS
Expedited Review
N

Advisory Committee Statement

Approval for updating Cologuard labeling to include the completed Post-Approval study information.

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