FDA device listing
Discovery 670 DR,Discovery NM/CT 670,Discovery NM/CT 670 ES,Discovery NM/CT 670 Pro,NM/CT 870 DR
FDA device listing 1656157457 · GE HealthCare Technologies Inc.
Key facts
| Proprietary names | Discovery 670 DR,Discovery NM/CT 670,Discovery NM/CT 670 ES,Discovery NM/CT 670 Pro,NM/CT 870 DR |
|---|---|
| Owner/operator | GE HealthCare Technologies Inc. |
| Owner/operator number | 9912004 |
| Premarket submissions | K093514 |
| Product codes | JAK, KPS |
| Device names | JAK - System, X-Ray, Tomography, Computed, KPS - System, Tomography, Computed, Emission |
| Device class | Class II |
| Classification regulations (21 CFR) | 892.1200, 892.1750 |
| Review panels | Radiology |
| Registered establishments | GE HANGWEI MEDICAL SYSTEMS CO., LTD., GE Medical Systems Israel, Functional Imaging, GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING |
| Establishment registrations | 9613299, 9613445, 3027338963, 3033524251 |
| FEI numbers | 3002175190, 3004571294, 3027338963, 3033524251 |
| Establishment operations | Manufacturer, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 UDI devices (GUDID) under the same submission
- 10–99 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