Catalog Number

-

Brand Name

Evolution4K

Version/Model Number

Evo4K130

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 30, 2020

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LMB

Product Code Name

Device, Digital Image Storage, Radiological

Public Device Record Key

1c2ecfb5-0347-4c2a-809d-bd406d44230b

Public Version Date

July 13, 2020

Public Version Number

5

DI Record Publish Date

March 04, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-