FDA Device Establishments · JSON-LD · Markdown
FEI 3003521780 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3003521780 |
|---|---|
| Owner / Operator | DEFIBTECH, LLC (#9048526) |
| Address | 741 BOSTON POST ROAD,SUITE 201, GUILFORD, CT, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | DRM |
| Regulation § (21 CFR) | 870.5200 |
| Proprietary names | Lifeline ARM ACC System; RMU-1000 Automated Chest Compressor (ACC) System |
Source: openFDA. Public-domain (CC0).