FDA Device Establishments · JSON-LD · Markdown
FEI 3012552532 · Export Device to the United States But Perform No Other Operation on Device Repack or Relabel Medical Device · Status: Active
| FEI Number | 3012552532 |
|---|---|
| Owner / Operator | ABBOTT LABORATORIES (#1415939) |
| Address | BruCargo 831, BruCargo Vlaams Brabant, 1931, BE |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | OAD, LPB |
| Proprietary names | Ampere Generator; FlexAbility Ablation Catheter; Sensor Enabled Ablation Connection Cable; Therapy Cool Flex Ablation Catheter; FlexAbility Ablation Catheter, Sensor Enabled; Safire BLU Duo Ablation Catheter; IBI 1500T9-CP V1.6 Cardiac Ablation Generator; Therapy Cool Path Duo Ablation Catheter; Ampere Generator Accessories; Ampere Footswitch |
Source: openFDA. Public-domain (CC0).