510(k) K253012

Device
AlignRT Plus (8.0)
Applicant
Vision Rt, Ltd.
510(k) number
K253012
Product code
IYE
Decision
Substantially Equivalent (SESE)
Decision date
2026-03-18
Date received
2025-09-19
Regulation
892.5050
Classification name
Accelerator, Linear, Medical
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Chelsey Moore
Address
Dove House, Arcadia Ave. London GB N3 2JU N3 2JU

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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K250696AccuCheckManteia Technologies Co., Ltd.2025-10-24
K250911MOSkin Radiation Measurement SystemElectrogenics Labs, Ltd.2025-10-17
K252948TrueBeam, TrueBeam STX, Edge and VitalBeamVarian Medical Systems, Inc.2025-10-07
K252174AquaCast MaskBlessing Cathay Corporation2025-09-03
K243142Cranial 4Pi ImmobilizationBrainlab AG2025-06-23
K243301MapRTVision Rt, Ltd.2025-05-19