# Abbott Medical

FEI: 3009600098
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: ABBOTT LABORATORIES (#1415939)

Address: 4 Robbins Rd, Westford, MA, US



## Products

Total registered: 3
Top product codes: DSK, NQQ, DQK
Regulation §: 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: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223009600098%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3009600098
