Catalog Number

-

Brand Name

Easy@Home TENS Pain Relief Device

Version/Model Number

EHE009

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

K131921,K131921

Product Code

NUH

Product Code Name

Stimulator, Nerve, Transcutaneous, Over-The-Counter

Public Device Record Key

0e8b9938-178a-4cb5-8b58-1d3804d28ca4

Public Version Date

July 23, 2020

Public Version Number

5

DI Record Publish Date

August 03, 2016

Package DI Number

10850253007120

Quantity per Package

20

Contains DI Package

00850253007123

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-