PMA supplement
P190032 S030: FoundationOne Liquid CDx (F1 Liquid CDx)
FDA PMA supplement · 135 Review Track For 30-Day Notice · Foundation Medicine, Inc.
Key facts
| Original PMA | P190032 |
|---|---|
| Supplement number | S030 |
| Supplement type | 135 Review Track For 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | FoundationOne Liquid CDx (F1 Liquid CDx) |
| Generic name | Next generation sequencing oncology panel, somatic or germline variant detection system |
| Applicant | Foundation Medicine, Inc. |
| Product code | PQP |
| Received date | Jan 30, 2025 |
| Decision date | Aug 12, 2026 |
At a glance
- No Expedited review granted
- No Approval order on file
- No Summary of safety and effectiveness on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA supplements
A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: