FDA device listing
Natus Neuroworks,Neuroworks
FDA device listing 1864721404 · Natus Medical Incorporated
Key facts
| Proprietary names | Natus Neuroworks,Neuroworks |
|---|---|
| Owner/operator | Natus Medical Incorporated |
| Owner/operator number | 9004873 |
| Premarket submissions | K180421 |
| Product codes | OLT, OMA, OMB |
| Device names | OLT - Non-Normalizing Quantitative Electroencephalograph Software, OMA - Amplitude-Integrated Electroencephalograph, OMB - Automatic Event Detection Software For Full-Montage Electroencephalograph |
| Device class | Class II |
| Classification regulations (21 CFR) | 882.1400 |
| Review panels | Neurology |
| Registered establishments | NATUS MEDICAL INCORPORATED DBA EXCEL-TECH LTD. (XLTEK) |
| Establishment registrations | 9612330 |
| FEI numbers | 3002809369 |
| Establishment operations | Complaint File Establishment, 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