FCRView - FCRView (CR-VW 674) is a Workstation intended to - FUJIFILM CORPORATION

Duns Number:713565195

Device Description: FCRView (CR-VW 674) is a Workstation intended to associate FCR images with patient and exa FCRView (CR-VW 674) is a Workstation intended to associate FCR images with patient and exam information, apply images processing to facilitate diagnosis, display the images, and output the resulting image and exam data for further display, distribution, or archiving. In addition, the FCR Viewcan receive DICOM multi modality images for viewing. The FCR View must not be used for primary diagnosis of mammography images.

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More Product Details

Catalog Number

-

Brand Name

FCRView

Version/Model Number

CR-VW674

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K081308

Product Code Details

Product Code

LLZ

Product Code Name

System, image processing, radiological

Device Record Status

Public Device Record Key

ee1a0427-c6ce-470f-afdb-34416fce3dd7

Public Version Date

February 21, 2019

Public Version Number

4

DI Record Publish Date

September 16, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"FUJIFILM CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 43
2 A medical device with a moderate to high risk that requires special controls. 324
3 A medical device with high risk that requires premarket approval 1