FDA device listing
ADVIA 120,ADVIA 120/2120
FDA device listing 1872207060 · SIEMENS HEALTHCARE DIAGNOSTICS INC.
Key facts
| Proprietary names | ADVIA 120,ADVIA 120/2120 |
|---|---|
| Owner/operator | SIEMENS HEALTHCARE DIAGNOSTICS INC. |
| Owner/operator number | 9096044 |
| Premarket submissions | K971998 |
| Product codes | GKL, GKZ |
| Device names | GKL - Counter, Cell, Automated (Particle Counter), GKZ - Counter, Differential Cell |
| Device class | Class II |
| Classification regulations (21 CFR) | 864.5200, 864.5220 |
| Review panels | Hematology |
| Registered establishments | Siemens Healthcare Diagnostics Inc., Siemens Healthcare Diagnostics Manufacturing Ltd. |
| Establishment registrations | 2432235, 8020888 |
| FEI numbers | 2432235, 3007019572 |
| Establishment operations | Complaint File Establishment, Specification Developer, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 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