510(k) K260192

Device
DIANA
Applicant
ROPCA ApS
510(k) number
K260192
Product code
QIH
Decision
Substantially Equivalent (SESE)
Decision date
2026-07-24
Date received
2026-01-22
Regulation
892.2050
Classification name
Automated Radiological Image Processing Software
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Trine Straarup Winther
Address
Cortex Park 26 E Odense M DK 5230 5230

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code QIH#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K261349SwiftMRAirs Medical, Inc.2026-07-24
K254096VELMENI for DENTISTS (V4D) 3DVelmeni, Inc.2026-07-23
K261535Hi-D Imaging 4TAVRHi-D Imaging AG2026-07-20
K260206SkeletonPlannerUPlanner B.V. - Presurgeo2026-07-15
K260973InferOperate SuiteBeijing Infervision Healthcare Medical Technology Co., Ltd.2026-07-07
K253628Auto-Seg (SO-0012), Spine Auto-Seg (SO-0012)Agada Medical, Ltd.2026-06-29
K253969ADAS 3DAdas3D Medical S.L.2026-06-29
K253786syngo.CT Coronary CockpitSiemens Medical Solutions USA, Inc.2026-06-25
K260316CMN Capillary Function with Oncology Virtual ExpertCercare Medical A/S2026-06-22
K261713Synapse PACS (7.6.0)FUJIFILM Healthcare Americas Corporation2026-06-18
K253172MediAI-OACrescom Co., Ltd.2026-06-15
K253690LungMapsSiemens Healthineers AG2026-06-15
K260300WatchMate SoftwareAnumana, Inc.2026-06-15
K260406Brainomix 360 HyperdensityBrainomix Limited2026-06-12
K260322Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX)Mighty Oak Medical2026-06-11