Catalog Number

-

Brand Name

VEA

Version/Model Number

AIX21000

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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

K211987

Product Code

LLZ

Product Code Name

System, image processing, radiological

Public Device Record Key

7f7fd0ca-db18-4ddc-a1ad-e982a1e53e84

Public Version Date

July 07, 2022

Public Version Number

1

DI Record Publish Date

June 29, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-