Lvb Abp-1306 Pro
by Huizhou LVB Maternal & Infant Supplies Co., Ltd.
Lvb Abp-1306 Pro is a Class II device made by Huizhou LVB Maternal & Infant Supplies Co., Ltd., cleared under FDA 510(k) K241004 on 11 Sep 2024 and listed in FDA GUDID since 19 Sep 2024 (UDI-DI 06935883913076), 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 | Number06935883913076 | Date19 Sep 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK241004 | Date11 Sep 2024 | StatusActive |
Official records
- AccessGUDID record 06935883913076
- FDA 510(k) database K241004
Across registries
- FDA 510(k) K241004 decided 11 Sep 2024 Active
- FDA GUDID UDI-DI 06935883913076 listed 19 Sep 2024 Listed
Timeline
- Cleared FDA 510(k) K241004
- Listed FDA GUDID 06935883913076
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Lvb
- Generic name
- Breast pump, electric
- Model / reference
- ABP-1306 PRO
- Primary DI / UDI-DI
- 06935883913076
- 510(k) Number
- FDA product code
- HGX
- GMDN term
- Breast pump, electric
- Device class
- Class II
- Regulation number
- 884.5160
- GUDID distribution status
- In Commercial Distribution
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