FDA device listing
Alinity i CEA Calibrators (LN 07P6201),Alinity i CEA Controls (LN 07P6210),Alinity i CEA Reagent Kit (LN 07P6220…
FDA device listing 1059413930 · ABBOTT LABORATORIES
Key facts
| Proprietary names | Alinity i CEA Calibrators (LN 07P6201),Alinity i CEA Controls (LN 07P6210),Alinity i CEA Reagent Kit (LN 07P6220, 07P6230),ARCHITECT CEA Calibrators (LN 7K68-02),ARCHITECT CEA Controls (LN 7K68-12),ARCHITECT CEA Reagent Kit (LN 7K68-27, 7K68-32, 7K68-35) |
|---|---|
| Owner/operator | ABBOTT LABORATORIES |
| Owner/operator number | 1415939 |
| Premarket submissions | K990774 |
| Product codes | DHX |
| Device names | DHX - System, Test, Carcinoembryonic Antigen |
| Device class | Class II |
| Classification regulations (21 CFR) | 866.6010 |
| Review panels | Immunology |
| Registered establishments | ABBOTT GmbH, ABBOTT IRELAND, ABBOTT LABORATORIES |
| Establishment registrations | 3002809144, 3005333358, 3008344661 |
| FEI numbers | 3002809144, 3005333358, 3008344661 |
| Establishment operations | Complaint File Establishment, Foreign Exporter, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None 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