FDA Device Establishments · JSON-LD · Markdown
FEI 1221363 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 1221363 |
|---|---|
| Owner / Operator | DIAGNOSYS LLC (#1221363) |
| Address | 55 TECHNOLOGY DR STE 100, Lowell, MA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HLZ |
| Regulation § (21 CFR) | 886.1220 |
| Proprietary names | DTL Plus Electrode |
Source: openFDA. Public-domain (CC0).