Catalog Number

AG8019

Brand Name

ICU Medical

Version/Model Number

AG8019

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"

Yes

For Single-Use

Yes

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

K932141,K932141

Product Code

DQO

Product Code Name

Catheter, intravascular, diagnostic

Public Device Record Key

5c1f6338-0015-4cbb-923a-906649179aff

Public Version Date

September 06, 2021

Public Version Number

1

DI Record Publish Date

August 29, 2021

Package DI Number

10840619060968

Quantity per Package

10

Contains DI Package

00840619060961

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS