BP-BT Kiosk
510(k) K200287
BP-BT Kiosk is a Class II device made by Ld Technology, LLC, cleared under FDA 510(k) K200287 on 15 May 2020, 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 | NumberK200287 | Date15 May 2020 | StatusActive |
Official records
- FDA 510(k) database K200287
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- DXN
- Device class
- Class II
- Regulation
- 21 CFR Part 870.1130
- Advisory committee
- Cardiovascular
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K200287
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 | |||
|---|---|---|---|---|
| BP-BT Lifeprobes Kiosk E001 | E001 | B322E0011 | — | On the market |
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