FDA Device Establishments · JSON-LD · Markdown
FEI 3030407739 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3030407739 |
|---|---|
| Owner / Operator | CL Medix Inc (#10089827) |
| Address | 14502 Lee Rd, Unit C, Chantilly, VA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | ISA |
| Regulation § (21 CFR) | 890.5660 |
| Proprietary names | MiracleWave Plus; The Miracle Wave HP200; The Miracle Wave F1; The Miracle Wave HP50; The Miracle Wave HandyWave |
Source: openFDA. Public-domain (CC0).