510(k) K231955

Device
aprevo® Digital Segmentation
Applicant
Carlsmed, Inc.
510(k) number
K231955
Product code
QIH
Decision
Substantially Equivalent (SESE)
Decision date
2023-11-03
Date received
2023-07-03
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
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Karen Liu
Address
1800 Aston Ave. Suite 100 Carlsbad CA US 92008 92008

FDA Registration Numbers

Source Documents

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

Related GUDID Devices

Primary DIBrandCompanyPublished
00810056991357aprevoCarlsmed, Inc.2026-01-15

Other 510(k) Records For Product Code QIH

510(k)DeviceApplicantDecision date
K261289UNiD™ Spine Analyzer (SW3002)Medicrea International S.A.S. (Medtronic)2026-05-15
K261273Neurophet AQUANeurophet., Inc.2026-05-15
K252563Neurophet SCALE PETNeurophet., Inc.2026-05-15
K254120SubtleHD-CT (1.x)Subtle Medical, Inc.2026-05-15
K260032MorphBeauBrain Healthcare, Inc.2026-05-13
K254189Synapse 3D Base Tools (V7.2)Fujifilm Corporation2026-04-30
K254184syngo Application SoftwareSiemens Medical Solutions USA, Inc.2026-04-29
K260785DS Core CBCT AnatomyDentsply Sirona2026-04-23
K253077uOmnispace.MRShanghai United Imaging Healthcare Co., Ltd.2026-04-22
K252332FolliscanMim Fertility2026-04-20
K253502Critical Care Suite with Enteric Tube Positioning AI AlgorithmGe Medical Systems, LLC2026-04-14
K252708Relu CloudRelu BV2026-04-10
K253930Overjet Iris Intelligent Imaging SystemOverjet, Inc.2026-04-10
K253689syngo Dynamics (VA41F)Siemens Healthcare GmbH2026-04-10
K254015CoLumbo C-SpineSmart Soft Healthcare AD2026-04-01