FDA Device Establishments · JSON-LD · Markdown
FEI 3023949424 · Manufacture Medical Device · Status: Active
| FEI Number | 3023949424 |
|---|---|
| Owner / Operator | Qurasense, Inc. (#10085929) |
| Address | 3517 Edison Way, Ste. D, Menlo Park, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | QZG, LCP |
| Regulation § (21 CFR) | 862.1675, 864.7470 |
| Proprietary names | A1c Q-Pad Kit; Q-Pad Kit; Q-Pad Collection Kit; Q-Pad Test System |
Source: openFDA. Public-domain (CC0).