Catalog Number

-

Brand Name

NA

Version/Model Number

NA

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

K160138,K160138,K160138

Product Code

GXY

Product Code Name

Electrode, Cutaneous

Public Device Record Key

a733e3a0-214a-4a8b-af02-4710c337b881

Public Version Date

February 19, 2021

Public Version Number

4

DI Record Publish Date

September 19, 2017

Package DI Number

06970341677381

Quantity per Package

420

Contains DI Package

06970341670337

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

paper carton