FDA Device Establishments · JSON-LD · Markdown
FEI 3005369540 · Manufacture Device in the United States for Export Only · Status: Active
| FEI Number | 3005369540 |
|---|---|
| Owner / Operator | MiraVista Diagnostics (#10077725) |
| Address | 4705 Decatur Boulevard, Indianapolis, IN, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MIZ |
| Regulation § (21 CFR) | 866.3320 |
| Proprietary names | Histoplasma urine antigen control kit; Histoplasma urine antigen LFA test kit |
Source: openFDA. Public-domain (CC0).