Natus 10392
by Xltek
Natus 10392 is a Class II device made by Xltek, cleared under FDA 510(k) K131266 on 14 Feb 2014 and listed in FDA GUDID since 20 Jul 2021 (UDI-DI 00382830002530), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00382830002530 | Date20 Jul 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK131266 | Date14 Feb 2014 | StatusActive |
Official records
- AccessGUDID record 00382830002530
- FDA 510(k) database K131266
Across registries
- FDA 510(k) K131266 decided 14 Feb 2014 Active
- FDA GUDID UDI-DI 00382830002530 listed 20 Jul 2021 Listed
Timeline
- Cleared FDA 510(k) K131266
- Listed FDA GUDID 00382830002530
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Natus
- Generic name
- Electroencephalograph
- Model / reference
- 10392
- Primary DI / UDI-DI
- 00382830002530
- 510(k) Number
- FDA product code
- GWQ
- GMDN term
- Electroencephalograph
- Device class
- Class II
- Regulation number
- 882.1400
- GUDID distribution status
- In Commercial Distribution
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