FDA device listing
GE 3.0T General Purpose Flex Coil
FDA device listing 1327814682 · GE HealthCare Technologies Inc.
Key facts
| Proprietary names | GE 3.0T General Purpose Flex Coil |
|---|---|
| Owner/operator | GE HealthCare Technologies Inc. |
| Owner/operator number | 9912004 |
| Premarket submissions | K030953 |
| Product codes | MOS |
| Device names | MOS - Coil, Magnetic Resonance, Specialty |
| Device class | Class II |
| Classification regulations (21 CFR) | 892.1000 |
| Review panels | Radiology |
| Registered establishments | GE Healthcare Coils, GE MEDICAL SYSTEMS, LLC, WIPRO GE HEALTHCARE PRIVATE LTD |
| Establishment registrations | 1529041, 2183553, 9613936 |
| FEI numbers | 2183553, 1000571342, 3005214683 |
| Establishment operations | Manufacturer, Specification Developer |
| 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