FDA Device Establishments · JSON-LD · Markdown
FEI 3015529603 · Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3015529603 |
|---|---|
| Owner / Operator | ElectroCore, Inc. (#10038007) |
| Address | 200 Forge Way, Suite 205, Rockaway, NJ, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | QAK, PKR |
| Regulation § (21 CFR) | 882.5892 |
| Proprietary names | gammaCore Sapphire 3; gammaCore Sapphire; gammaCore Sapphire SLC; gammaCore Sapphire D |
Source: openFDA. Public-domain (CC0).