Catalog Number

-

Brand Name

TRUEcontrol

Version/Model Number

TRUEcontrol Solution Level 0

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K032657,K032657,K032657

Product Code

JJX

Product Code Name

Single (Specified) Analyte Controls (Assayed And Unassayed)

Public Device Record Key

8668f78d-926d-4a4a-b6c5-fd2102a01a8c

Public Version Date

November 01, 2021

Public Version Number

2

DI Record Publish Date

January 29, 2021

Package DI Number

00021292002091

Quantity per Package

1

Contains DI Package

00021292008383

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX