Veuron-Brain-pAb3
510(k) K231642
Veuron-Brain-pAb3 is a medical device (FDA Class II; FDA product code LLZ, System, Image Processing, Radiological) made by Heuron Co., Ltd., cleared under FDA 510(k) K231642 on 13 Oct 2023, 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 | FDA 510(k)SESE | NumberK231642 | Date13 Oct 2023 | StatusActive |
Official records
- FDA 510(k) database K231642
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LLZ
- Device class
- Class II
- Regulation
- 21 CFR Part 892.2050
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K231642
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| Veuron-Brain-pAb3 AD-AWC03 | AD-AWC03 | 08800086200408 | — | On the market |
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