PMA supplement
P190032 S025: FoundationOne®Liquid CDx
FDA PMA supplement · Normal 180 Day Track No User Fee · Foundation Medicine, Inc.
Key facts
| Original PMA | P190032 |
|---|---|
| Supplement number | S025 |
| Supplement type | Normal 180 Day Track No User Fee |
| Reason for the supplement | Location Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | FoundationOne®Liquid CDx |
| Generic name | Next generation sequencing oncology panel, somatic or germline variant detection system |
| Applicant | Foundation Medicine, Inc. |
| Product code | PQP |
| Received date | Sep 18, 2024 |
| Decision date | May 8, 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: