FDA device listing
B38858 URINE/CSF ALBUMIN,B38859 URINE/CSF ALBUMIN CALIBRATOR,B46435 URINE/CSF ALBUMIN
FDA device listing 1836599537 · BECKMAN COULTER, INC.
Key facts
| Proprietary names | B38858 URINE/CSF ALBUMIN,B38859 URINE/CSF ALBUMIN CALIBRATOR,B46435 URINE/CSF ALBUMIN |
|---|---|
| Owner/operator | BECKMAN COULTER, INC. |
| Owner/operator number | 2050012 |
| Premarket submissions | K142346 |
| Product codes | DCF, JIT |
| Device names | DCF - Albumin, Antigen, Antiserum, Control, JIT - Calibrator, Secondary |
| Device class | Class II |
| Classification regulations (21 CFR) | 862.1150, 866.5040 |
| Review panels | Clinical Chemistry, Immunology |
| Registered establishments | Beckman Coulter Ireland Inc |
| Establishment registrations | 9680746 |
| FEI numbers | 1000206808 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 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