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

K092546,K160138,K092546,K160138

Product Code

GXY

Product Code Name

Electrode, Cutaneous

Public Device Record Key

64fba241-d4b0-417e-8888-064ff12ba5bd

Public Version Date

February 19, 2021

Public Version Number

4

DI Record Publish Date

October 12, 2016

Package DI Number

06970341677121

Quantity per Package

100

Contains DI Package

06970341674144

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

paper carton