FoundationOne®Liquid CDx (F1LCDx)
FDA premarket approval P190032/S020 · decided 2024-04-16
Approval details
- PMA number
- P190032
- Supplement
- S020
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- FoundationOne®Liquid CDx (F1LCDx)
- Generic name
- Next generation sequencing oncology panel, somatic or germline variant detection system
- Applicant
- Foundation Medicine, Inc.
- Date received
- 2024-03-15
- Decision date
- 2024-04-16
- Days to decision
- 32 days
- Decision code
- OK30
- Product code
- PQP
- Advisory committee
- Pathology
- Expedited review
- No
- Location
- Boston, MA
- Statement
- using a modified AB1 QC release process to enable the temporary use of an AB1 Baitset
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