FDA Device Establishments · JSON-LD · Markdown
FEI 1938095 · Manufacture Medical Device · Status: Active
| FEI Number | 1938095 |
|---|---|
| Owner / Operator | SURE-TECH DIAGNOSTIC ASSOCIATES, INC. (#1938095) |
| Address | 12115 Tesson Ferry Professional Ctr, Saint Louis, MO, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GHQ |
| Regulation § (21 CFR) | 864.7455 |
| Proprietary names | KLEIHAUER-BETKE KIT; FETAL HEMOGLOBIN KIT |
Source: openFDA. Public-domain (CC0).