FDA device listing
CardioLab AltiX AI.i,CardioLab AltiX XI,ComboLab AltiX AI.i,ComboLab AltiX XI,Mac-Lab AltiX AI.i,Mac-Lab AltiX XI,MLCL…
FDA device listing 1816403130 · GE HealthCare Technologies Inc.
Key facts
| Proprietary names | CardioLab AltiX AI.i,CardioLab AltiX XI,ComboLab AltiX AI.i,ComboLab AltiX XI,Mac-Lab AltiX AI.i,Mac-Lab AltiX XI,MLCL Client Software AltiX AI.i,MLCL Client Software AltiX XI |
|---|---|
| Owner/operator | GE HealthCare Technologies Inc. |
| Owner/operator number | 9912004 |
| Premarket submissions | K243540 |
| Product codes | DQK |
| Device names | DQK - Computer, Diagnostic, Programmable |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.1425 |
| Review panels | Cardiovascular |
| Registered establishments | GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, GE Medical Systems Information Technologies, Inc. |
| Establishment registrations | 1651104, 3001570235 |
| FEI numbers | 3001570235, 3002737156 |
| Establishment operations | Manufacturer, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database