BriefCase

BriefCase is a radiological computer aided triage and notification software device. Software version 1.1.0.0 for ICH triage.

Registry build 21.09.26
1manufacturer
3catalogue numbers in this listing
25510(k) clearances naming this product code

Who Else Makes It

Registered in Beijing.

Chinese manufacturers registered for FDA product code QAS
Manufacturer City Province Registered as Device types
Beijing Infervision Healthcare Medical Technology Co., Ltd. Beijing Beijing Complaint-file establishment 4

Record

Regulatory record for BriefCase
Listed by Aidoc Medical Ltd., Israel
FDA product code QAS
Device type Radiological Computer-Assisted Triage And Notification Software
Device class Class 2
Regulation 21 CFR 892.2080
Establishment Manufacturer
510(k) K180647
Record published 2019-09-01
Record revised 2026-02-12 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Latex Contains natural rubber latex
Label carries serial number
Distribution end date 2019-11-25

Catalogue Numbers

Catalogue numbers for BriefCase
Catalogue number Size Status
2.0.0 Withdrawn
3.0.0 Withdrawn
1.1.0.0 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Viz LVO Viz.ai, Inc. 12
Triage Stroke Brainomix Limited 5
BriefCase Triage Aidoc Medical Ltd. 5
Triage LVO Brainomix Limited 5
HealthICH Nano-X AI Ltd. 3
Annalise Triage Harrison-AI Medical Pty Ltd 3
Triage ICH Brainomix Limited 3
syngo.CT Brain Hemorrhage Siemens Healthcare Limited 2
AccipioIx Maxq AI Ltd 2
Viz ICH Viz.ai, Inc. 2
qER Qure.ai Technologies Private Limited 1
Viz SDH (Viz Subdural) Viz.ai, Inc. 1

Showing 12 of 29. All products under Radiological Computer-Assisted Triage And Notification Software

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K261317 2026-05-14
K253578 2026-02-26
K251195 2026-01-27
K252970 2026-01-07
K253265 2025-11-06
K251406 2025-05-30
K250248 2025-02-14
K242837 2024-10-18
K241727 2024-07-12
K232751 2023-10-30
K221330 2022-11-18
K220709 2022-10-07
K222329 2022-09-28
K222277 2022-08-26
K221314 2022-06-03
K221240 2022-05-17
K213886 2022-04-26
K213721 2022-03-21
K203508 2020-12-29
K201020 2020-08-26
K193298 2020-06-19
K192383 2019-12-20
K190896 2019-05-31
K190072 2019-04-15
K180647 2018-08-01

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer