FDA device listing
OSR6107 ALT,OSR6607 ALT
FDA device listing 1766184639 · BECKMAN COULTER, INC.
Key facts
| Proprietary names | OSR6107 ALT,OSR6607 ALT |
|---|---|
| Owner/operator | BECKMAN COULTER, INC. |
| Owner/operator number | 2050012 |
| Premarket submissions | K925339 |
| Product codes | CKA |
| Device names | CKA - Nadh Oxidation/Nad Reduction, Alt/Sgpt |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.1030 |
| Review panels | Clinical Chemistry |
| 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