Codonics Horizon® Multi-Media Imager

Grayscale/Color Desktop Small Format Film and Paper Diagnostic Imager - 51C

Registry build 21.09.26
2manufacturers in China registered for this device type
7catalogue numbers in this listing
6510(k) clearances naming this product code

Who Else Makes It

All of them in Jiangsu. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code LMC
Manufacturer City Province Registered as Device types
Qisda Electronics (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 5
Fujifilm Imaging System (Suzhou) Co., Ltd. Suzhou Jiangsu Manufacturer 3

Record

Regulatory record for Codonics Horizon® Multi-media Imager
Listed by Codonics, Inc., United States
FDA product code LMC
Device type Camera, Multi Format, Radiological
Device class Class 2
Regulation 21 CFR 892.2040
Establishment Remanufacturer, Complaint-file establishment, Manufacturer
510(k) K021054
Record published 2016-08-23
Record revised 2020-12-04 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Codonics Horizon® Multi-media Imager
Catalogue number Size Status
53C In distribution
51C In distribution
52C In distribution
150C In distribution
54C In distribution
55C In distribution
50C In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Fuji Medical DRY Film Fujifilm Corporation 13
Sony Sony Corporation 9
Dryview 5700 Laser Imaging System Carestream Health, Inc. 4
Dryview 5950 Laser Imaging System Carestream Health, Inc. 4
Codonics Horizon® Operating Software Codonics, Inc. 4
Drypro Model 873 Konica Minolta, Inc. 3
Drypro Model 832 Konica Minolta, Inc. 2
Drypix Plus Fujifilm Corporation 2
Drypro Sigma Konica Minolta, Inc. 2
Drypro Sigma 2 Konica Minolta, Inc. 2
Dryview 6950 Laser Imaging System Carestream Health, Inc. 2
Drypix Smart Fujifilm Corporation 2

Showing 12 of 29. All products under Camera, Multi Format, Radiological

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K060440 2006-03-16
K042232 2004-10-05
K030690 2003-04-30
K021054 2002-05-09
K003481 2001-01-19
K962364 1996-11-08

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