FDA Device Establishments · JSON-LD · Markdown
FEI 3030064535 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3030064535 |
|---|---|
| Owner / Operator | Buoy Software (#10089333) |
| Address | 811 Barton Springs Rd Ste 510, Austin, TX, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MMH |
| Regulation § (21 CFR) | 864.9165 |
| Proprietary names | Blood Product Questionnaire Module |
Source: openFDA. Public-domain (CC0).