FDA Device Establishments · JSON-LD · Markdown
FEI 1220973 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 1220973 |
|---|---|
| Owner / Operator | DEKA Research & Development Corp. (#10041884) |
| Address | 340 Commercial St, Manchester, NH, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | QFG, NDC |
| Regulation § (21 CFR) | 880.5730, 868.1890 |
Source: openFDA. Public-domain (CC0).