Atlas FDA

COLOGUARD

FDA premarket approval P130017/S009 · decided 2016-05-05

Approval details

PMA number
P130017
Supplement
S009
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
COLOGUARD
Generic name
System, colorectal neoplasia, DNA methylation and hemoglobin detection
Applicant
Exact Sciences Corporation
Date received
2016-04-14
Decision date
2016-05-05
Days to decision
21 days
Decision code
OK30
Product code
PHP
Advisory committee
Pathology
Expedited review
No
Location
Medison, WI
Statement
Qualify an alternative supplier for reagents utilized in the Cologuard assay.

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