FDA Device Establishments · JSON-LD · Markdown
FEI 3014527900 · Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device · Status: Active
| FEI Number | 3014527900 |
|---|---|
| Owner / Operator | DxNow, Inc. (#10057557) |
| Address | 401 Professional Drive, Suite 130, Gaithersburg, MD, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | MQK |
| Regulation § (21 CFR) | 884.6160 |
| Proprietary names | ZyMot Multi Sperm Separation Device; ZyMot ICSI Sperm Separation Device |
Source: openFDA. Public-domain (CC0).