Catalog Number

-

Brand Name

Arterys Viewer

Version/Model Number

AVM3

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 22, 2018

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

K171544

Product Code

LLZ

Product Code Name

System, Image Processing, Radiological

Public Device Record Key

6e8d10cc-3ed6-4b04-bab6-10dcd4fc61ad

Public Version Date

October 07, 2019

Public Version Number

9

DI Record Publish Date

November 01, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-