FDA device listing
NEUVO
FDA device listing 1900356533 · Compumedics USA Inc.
Key facts
| Proprietary names | NEUVO |
|---|---|
| Owner/operator | Compumedics USA Inc. |
| Owner/operator number | 9029712 |
| Premarket submissions | K081151 |
| Product codes | GWE, GWF, GWJ, GWQ |
| Device names | GWE - Stimulator, Photic, Evoked Response, GWF - Stimulator, Electrical, Evoked Response, GWJ - Stimulator, Auditory, Evoked Response, GWQ - Full-Montage Standard Electroencephalograph |
| Device class | Class II |
| Classification regulations (21 CFR) | 882.1400, 882.1870, 882.1890, 882.1900 |
| Review panels | Neurology |
| Registered establishments | COMPUMEDICS USA, INC. |
| Establishment registrations | 1650946 |
| FEI numbers | 3002716534 |
| Establishment operations | Complaint File Establishment, Repackager/Relabeler |
| 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