FDA Device Establishments · JSON-LD · Markdown
FEI 1000126037 · Manufacture Medical Device · Status: Active
| FEI Number | 1000126037 |
|---|---|
| Owner / Operator | AMERITEKUSA, INC. (#9002732) |
| Address | 125 130th St SE Ste 200, EVERETT, WA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | JHI |
| Regulation § (21 CFR) | 862.1155 |
| Proprietary names | dBest hCG 2 IU/ml Test Kit |
Source: openFDA. Public-domain (CC0).