FDA device listing
Kit, Test, Pregnancy, Hcg, Over The Counter
FDA device listing 1061927218 · ABBOTT LABORATORIES
Key facts
| Owner/operator | ABBOTT LABORATORIES |
|---|---|
| Owner/operator number | 1415939 |
| Product codes | LCX |
| Device names | LCX - Kit, Test, Pregnancy, Hcg, Over The Counter |
| Device class | Class II |
| Classification regulations (21 CFR) | 862.1155 |
| Review panels | Clinical Chemistry |
| Registered establishments | Abbott Diagnostics (Shanghai) Co., Ltd. |
| Establishment registrations | 3005128563 |
| FEI numbers | 3005128563 |
| Establishment operations | Contract Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed 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