FDA Device Establishments · JSON-LD · Markdown
FEI 3005853611 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3005853611 |
|---|---|
| Owner / Operator | Laboratory Corporation of America Holdings (#10049571) |
| Address | 500 Perimeter Park Drive, Suite B, Morrisville, NC, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MVU |
| Regulation § (21 CFR) | 864.4020 |
| Proprietary names | MGMT Forward Primer/Probe |
Source: openFDA. Public-domain (CC0).