Es-Bc F001
Es-Bc F001 is a Class II device made by LD Technology, cleared under FDA 510(k) K103026 on 29 Mar 2011 and listed in FDA GUDID since 5 Mar 2024 (UDI-DI B322F0011), 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 | NumberB322F0011 | Date5 Mar 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK103026 | Date29 Mar 2011 | StatusActive |
Official records
- FDA 510(k) database K103026
Across registries
- FDA 510(k) K103026 decided 29 Mar 2011 Active
- FDA GUDID UDI-DI B322F0011 listed 5 Mar 2024 Listed
Timeline
- Cleared FDA 510(k) K103026
- Listed FDA GUDID B322F0011
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Es-Bc
- Generic name
- Bioelectrical body composition analyser
- Model / reference
- F001
- Primary DI / UDI-DI
- B322F0011
- 510(k) Number
- FDA product code
- MNW
- GMDN term
- Bioelectrical body composition analyser
- Device class
- Class II
- Regulation number
- 870.2770
- GUDID distribution status
- In Commercial Distribution
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