LF900 LF90100-Bx
LF900 LF90100-Bx is a sequential venous compression system inflator (FDA Class II; FDA product code IRP, Massager, Powered Inflatable Tube) made by Daesung Maref Co., Ltd., cleared under FDA 510(k) K231437 on 19 Jul 2023 and listed in FDA GUDID since 20 May 2024 (UDI-DI 08809802644656), 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 | Number08809802644656 | Date20 May 2024 | StatusListed |
| United States | FDA 510(k) | NumberK231437 | Date19 Jul 2023 | StatusActive |
Official records
- AccessGUDID record 08809802644656
- FDA 510(k) database K231437
Across registries
- FDA 510(k) K231437 decided 19 Jul 2023 Active
- FDA GUDID UDI-DI 08809802644656 listed 20 May 2024 Listed
Timeline
- Cleared FDA 510(k) K231437
- Listed FDA GUDID 08809802644656
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- LF900
- Generic name
- Sequential venous compression system inflator
- Model / reference
- LF90100-BX
- Primary DI / UDI-DI
- 08809802644656
- 510(k) Number
- FDA product code
- IRP
- GMDN term
- Sequential venous compression system inflator
- Device class
- Class II
- Regulation number
- 890.5650
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Sequential venous compression system inflator.