Catalog Number

RF4019-01

Brand Name

TRUE METRIX GO

Version/Model Number

TRUE METRIX GO Self Monitoring Blood Glucose Meter

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LFR

Product Code Name

Glucose Dehydrogenase, Glucose

Public Device Record Key

62682713-0673-4a6d-b8ca-f71797c4132e

Public Version Date

November 12, 2018

Public Version Number

2

DI Record Publish Date

June 30, 2018

Package DI Number

10708820721095

Quantity per Package

12

Contains DI Package

00708820721098

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE