LineUp
510(k) K180727
LineUp is a Class II device made by CurveBeam LLC, cleared under FDA 510(k) K180727 on 11 May 2018, 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 | NumberK180727 | Date11 May 2018 | StatusActive |
Official records
- FDA 510(k) database K180727
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- JAK
- FDA applicant
- Curvebeam, LLC
- Device class
- Class II
- Regulation
- 21 CFR Part 892.1750
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K180727
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 | |||
|---|---|---|---|---|
| LineUP 1030-115 | 1030-115 | 00863152000348 | — | On the market |
| LineUP 1030-230 | 1030-230 | 00863152000355 | — | On the market |
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