FDA Device Establishments · JSON-LD · Markdown
FEI 3033274216 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3033274216 |
|---|---|
| Owner / Operator | RetMap, Inc. (#10091755) |
| Address | 832 W Superior St # 202e, Chicago, IL, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HLZ |
| Regulation § (21 CFR) | 886.1220 |
| Proprietary names | RM Electrode |
Source: openFDA. Public-domain (CC0).