FDA Device Establishments · JSON-LD · Markdown
FEI 3018382937 · Manufacture Medical Device · Status: Active
| FEI Number | 3018382937 |
|---|---|
| Owner / Operator | Mid-America Safety Corp (#10081267) |
| Address | 800 Greenleaf Ave, Elk Grove Village, IL, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FXX |
| Regulation § (21 CFR) | 878.4040 |
| Proprietary names | MASC |
Source: openFDA. Public-domain (CC0).