FDA Device Establishments · JSON-LD · Markdown
FEI 3004091615 · Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 3004091615 |
|---|---|
| Owner / Operator | ABBOTT LABORATORIES (#1415939) |
| Address | Argonstraat 1, Heerlen Limburg, 6422 PH, NL |
| Mandatory US Agent | Abbott Vascular |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | DQX |
| Regulation § (21 CFR) | 870.1330 |
| Proprietary names | Hi-Torque Versacore Floppy Guide Wire; Hi-Torque Versacore Standard Guide Wire; Hi-Torque Versacore Modified J Guide Wire; Hi-Torque Versacore Guide Wire |
Source: openFDA. Public-domain (CC0).