Catalog Number

-

Brand Name

Patient Set

Version/Model Number

640457

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

K151048,K151048,K151048

Product Code

IZQ

Product Code Name

Injector, Contrast Medium, Automatic

Public Device Record Key

92941a0f-ad7e-42e5-b0a6-2410313e083a

Public Version Date

April 07, 2021

Public Version Number

2

DI Record Publish Date

May 06, 2020

Package DI Number

37630039301317

Quantity per Package

25

Contains DI Package

17630039301313

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

box