Guardant360 CDx
FDA premarket approval P200010/S008 · decided 2022-08-11
Approval details
- PMA number
- P200010
- Supplement
- S008
- Supplement type
- Panel Track
- Supplement reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Trade name
- Guardant360 CDx
- Generic name
- Next generation sequencing oncology panel, somatic or germline variant detection system
- Applicant
- Guardant Health, Inc.
- Date received
- 2022-04-13
- Decision date
- 2022-08-11
- Days to decision
- 120 days
- Decision code
- APPR
- Product code
- PQP
- Advisory committee
- Pathology
- Expedited review
- No
- Location
- Redwood City, CA
- Statement
- Approval for expanding the indications for use to include the companion diagnostic claim to identify non-small cell lung cancer patients with ERBB2 activating mutations (SNVs and exon 20 insertions) for treatment with ENHERTU (fam-trastuzumab deruxtecan-nxki).
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