Catalog Number

572

Brand Name

Liquichek

Version/Model Number

572

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K002120

Product Code

JJS

Product Code Name

CONTROLS FOR BLOOD-GASES, (ASSAYED AND UNASSAYED)

Public Device Record Key

50f714c5-46f7-4115-a13c-af93b7b7f942

Public Version Date

July 29, 2021

Public Version Number

5

DI Record Publish Date

December 05, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-