FDA Device Establishments · JSON-LD · Markdown
FEI 3018387313 · Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 3018387313 |
|---|---|
| Owner / Operator | EM Device Lab, Inc. (#10081242) |
| Address | 6303 Mountain Park Cv, Austin, TX, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GBX |
| Regulation § (21 CFR) | 878.4200 |
| Proprietary names | Quickloop Abscess Treatment Device |
Source: openFDA. Public-domain (CC0).