Catalog Number

-

Brand Name

CADstream

Version/Model Number

7.0

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 21, 2021

Issuing Agency

In GS1

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K092954

Product Code

LLZ

Product Code Name

System, Image Processing, Radiological

Public Device Record Key

56d10b44-4ef0-467a-bb31-31a1cc3dcef7

Public Version Date

August 30, 2022

Public Version Number

2

DI Record Publish Date

September 21, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-