Atlas FDA

Guardant360 CDx

FDA premarket approval P200010/S009 · decided 2022-10-26

Approval details

PMA number
P200010
Supplement
S009
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Guardant360 CDx
Generic name
Next generation sequencing oncology panel, somatic or germline variant detection system
Applicant
Guardant Health, Inc.
Date received
2022-04-27
Decision date
2022-10-26
Days to decision
182 days
Decision code
APPR
Product code
PQP
Advisory committee
Pathology
Expedited review
No
Location
Redwood City, CA
Statement
Approval of the updates and revisions made to the Guardant360® CDx labeling documents.

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