FDA Device Establishments · JSON-LD · Markdown
FEI 3008782989 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 3008782989 |
|---|---|
| Owner / Operator | ClearFlow, Inc. (#10034650) |
| Address | 16 Technology Drive. Suite 150, Irvine, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | OTK, GBX |
| Regulation § (21 CFR) | 878.4780, 878.4200 |
| Proprietary names | PleuraFlow System with FlowGlide 20FR SEDL, PF-20 SEDL |
Source: openFDA. Public-domain (CC0).