FDA device listing
471080 SYNCHRON Systems Drug Calibrator 3 Plus
FDA device listing 1227027092 · BECKMAN COULTER, INC.
Key facts
| Proprietary names | 471080 SYNCHRON Systems Drug Calibrator 3 Plus |
|---|---|
| Owner/operator | BECKMAN COULTER, INC. |
| Owner/operator number | 2050012 |
| Premarket submissions | K971287 |
| Product codes | DKB |
| Device names | DKB - Calibrators, Drug Mixture |
| Device class | Class II |
| Classification regulations (21 CFR) | 862.3200 |
| Review panels | Clinical Toxicology |
| Registered establishments | BECKMAN COULTER, INC. |
| Establishment registrations | 2050010, 2050012 |
| FEI numbers | 2050010, 2050012 |
| Establishment operations | Contract Manufacturer, 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