FDA device listing
Alinity m EBV AMP Kit,Alinity m EBV Application Specification File,Alinity m EBV CAL Kit,Alinity m EBV CTRL Kit
FDA device listing 2045324722 · ABBOTT LABORATORIES
Key facts
| Proprietary names | Alinity m EBV AMP Kit,Alinity m EBV Application Specification File,Alinity m EBV CAL Kit,Alinity m EBV CTRL Kit |
|---|---|
| Owner/operator | ABBOTT LABORATORIES |
| Owner/operator number | 1415939 |
| Premarket submissions | K212778 |
| Product codes | QLX |
| Device names | QLX - Nucleic Acid Amplification Test For The Quantitation Of Epstein-Barr Virus (Ebv) Dna |
| Device class | Class II |
| Classification regulations (21 CFR) | 866.3183 |
| Review panels | Microbiology |
| Registered establishments | ABBOTT MOLECULAR, INC. |
| Establishment registrations | 3005248192 |
| FEI numbers | 3005248192 |
| Establishment operations | Manufacturer |
| 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