FDA Device Establishments · JSON-LD · Markdown
FEI 2084025 · Manufacture Medical Device · Status: Active
| FEI Number | 2084025 |
|---|---|
| Owner / Operator | KAMIYA BIOMEDICAL COMPANY LLC (#9001370) |
| Address | 12779 Gateway Dr S, Tukwila, WA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | GTQ |
| Regulation § (21 CFR) | 866.3720 |
| Proprietary names | K-ASSAY(R) ASO Calibrator; K-ASSAY(R) ASO |
Source: openFDA. Public-domain (CC0).