ClearRead CT Docker

ClearRead CT on Docker Platform. Original Commercial Distribution Date: 2020-05-19. Mistyped as M722CD20105V20040.

Registry build 21.09.26
1manufacturer
14catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Registered in Beijing.

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

Record

Regulatory record for ClearRead CT Docker
Listed by Riverain Technologies, United States
FDA product code OEB
Device type Lung Computed Tomography System, Computer-Aided Detection
Device class Class 2
Regulation 21 CFR 892.2050
Establishment Manufacturer
Premarket notification Exempt
Record published 2022-01-28
Record revised 2023-10-18 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries serial number
Distribution end date 2020-12-30

Catalogue Numbers

Catalogue numbers for ClearRead CT Docker
Catalogue number Size Status
5.2.0 In distribution
5.0.0 In distribution
5.8.0 In distribution
5.6.1 In distribution
5.6.2 In distribution
5.7.0 In distribution
1.1.0 In distribution
5.5.0 In distribution
5.8.1 In distribution
5.6.0 In distribution
5.6.3 In distribution
1.2.0 In distribution
1.1.0 Withdrawn
1.2.0 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
ClearRead CT Console Riverain Technologies 20
ClearRead CT Server Riverain Technologies 16
ClearRead CT Riverain Technologies 11
ClearRead CT Platform Docker Riverain Technologies 7
Veolity Mevis Medical Solutions AG 2
Veolity LungCAD Mevis Medical Solutions AG 2
Visia LungCAD Mevis Medical Solutions AG 2
DynaCAD Lung Server Mevis Medical Solutions AG 2
InferRead Lung Ct.ai 2.1.2.1 Infervision US Inc 1
InferRead Lung Ct.ai Infervision Medical Technology Co., Ltd. 1
Aview Lung Nodule CAD Coreline Soft Co., Ltd. 1
DynaCAD Lung Mevis Medical Solutions AG 1

Showing 12 of 13. All products under Lung Computed Tomography System, Computer-Aided Detection

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K221612 2022-12-05
K161201 2016-09-09

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