Atlas FDA

Guardant360 CDx

FDA premarket approval P200010/S028 · decided 2025-12-29

Approval details

PMA number
P200010
Supplement
S028
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Guardant360 CDx
Generic name
Next generation sequencing oncology panel, somatic or germline variant detection system
Applicant
Guardant Health, Inc.
Date received
2025-11-26
Decision date
2025-12-29
Days to decision
33 days
Decision code
OK30
Product code
PQP
Advisory committee
Pathology
Expedited review
No
Location
Redwood City, CA
Statement
approval of manufacturing room changes

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