Kernel KN-4003AL2DS
by Xuzhou Kernel Medical Equipment Co., Ltd.
Kernel KN-4003AL2DS is a Class II device made by Xuzhou Kernel Medical Equipment Co., Ltd., cleared under FDA 510(k) K181805 on 11 Jan 2019 and listed in FDA GUDID since 8 Mar 2019 (UDI-DI 06928798600131), active as of 22 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 | Number06928798600131 | Date8 Mar 2019 | StatusListed |
| United States | FDA 510(k) | NumberK181805 | Date11 Jan 2019 | StatusActive |
Official records
- AccessGUDID record 06928798600131
- FDA 510(k) database K181805
Across registries
- FDA 510(k) K181805 decided 11 Jan 2019 Active
- FDA GUDID UDI-DI 06928798600131 listed 8 Mar 2019 Listed
Timeline
- Cleared FDA 510(k) K181805
- Listed FDA GUDID 06928798600131
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Kernel
- Generic name
- Ultraviolet phototherapy unit, home-use
- Model / reference
- KN-4003AL2DS
- Primary DI / UDI-DI
- 06928798600131
- 510(k) Number
- FDA product code
- FTC
- GMDN term
- Ultraviolet phototherapy unit, home-use
- Device class
- Class II
- Regulation number
- 878.4630
- GUDID distribution status
- In Commercial Distribution
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