Catalog Number

-

Brand Name

Transtek

Version/Model Number

LS202-B

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

MNW

Product Code Name

Analyzer, Body Composition

Public Device Record Key

7c4ccf2b-580e-46e6-8cc2-c1e268ec7ed3

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

January 05, 2017

Package DI Number

14714781444665

Quantity per Package

1

Contains DI Package

04714781444668

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box