Catalog Number

-

Brand Name

Balance

Version/Model Number

0386

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

76a2b456-7fb9-4f95-bf6d-2dc4ffa3d17f

Public Version Date

July 09, 2018

Public Version Number

1

DI Record Publish Date

June 06, 2018

Package DI Number

10875011003862

Quantity per Package

4

Contains DI Package

00875011003865

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Carton