FDA device listing
443360 Synchron CX Calibration Standard 1,443365 Synchron CX Calibration Standard 2
FDA device listing 1194304143 · BECKMAN COULTER, INC.
Key facts
| Proprietary names | 443360 Synchron CX Calibration Standard 1,443365 Synchron CX Calibration Standard 2 |
|---|---|
| Owner/operator | BECKMAN COULTER, INC. |
| Owner/operator number | 2050012 |
| Premarket submissions | K864236 |
| Product codes | JIX, JJF |
| Device names | JIX - Calibrator, Multi-Analyte Mixture, JJF - Analyzer, Chemistry, Micro, For Clinical Use |
| Device class | Class I, Class II |
| Classification regulations (21 CFR) | 862.1150, 862.2170 |
| Review panels | Clinical Chemistry |
| Registered establishments | BECKMAN COULTER, INC. |
| Establishment registrations | 2050012 |
| FEI numbers | 2050012 |
| Establishment operations | Specification Developer |
| 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