Catalog Number

A4054-75

Brand Name

TRUEtrack

Version/Model Number

TRUEtrack PRE-PACK

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

January 31, 2017

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K032657

Product Code

CGA

Product Code Name

Glucose Oxidase, Glucose

Public Device Record Key

389f235c-20e8-437e-8419-85195a1bf16e

Public Version Date

November 01, 2021

Public Version Number

3

DI Record Publish Date

September 20, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-