Guardant360® CDx
FDA premarket approval P200010/S011 · decided 2022-07-29
Approval details
- PMA number
- P200010
- Supplement
- S011
- 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
- 2022-07-01
- Decision date
- 2022-07-29
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- PQP
- Advisory committee
- Pathology
- Expedited review
- No
- Location
- Redwood City, CA
- Statement
- Relocation of the manufacturing room for reagent components.
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