FDA Device Establishments · JSON-LD · Markdown
FEI 3009600098 · Manufacture Medical Device · Status: Active
| FEI Number | 3009600098 |
|---|---|
| Owner / Operator | ABBOTT LABORATORIES (#1415939) |
| Address | 4 Robbins Rd, Westford, MA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 3 |
| Product codes (top 20) | DSK, NQQ, DQK |
| Regulation § (21 CFR) | 870.1110, 892.1560, 870.1425 |
| Proprietary names | Optis Next Upgrade Kit; Optis Integrated Next; Optis Tableside Controller Next; Ultreon 2 Software Upgrade Kit; Optis Integrated Pre-Install Kit; Optis Mobile Next Imaging System; OPTIS Mobile Next; Optis Mobile Next Direct Upgrade Accessory Kit |
Source: openFDA. Public-domain (CC0).