FDA Device Establishments · JSON-LD · Markdown
FEI 1832216 · Manufacture Device in the United States for Export Only · Status: Active
| FEI Number | 1832216 |
|---|---|
| Owner / Operator | TECO DIAGNOSTICS (#1832216) |
| Address | 1268 NORTH LAKEVIEW AVE., ANAHEIM, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | CEP |
| Regulation § (21 CFR) | 862.1485 |
| Proprietary names | LH Elisa Test kit |
Source: openFDA. Public-domain (CC0).