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

1630d523-944d-4f49-9ec0-91454ebfc722

Public Version Date

July 23, 2020

Public Version Number

2

DI Record Publish Date

February 03, 2020

Package DI Number

10810038630110

Quantity per Package

20

Contains DI Package

00810038630113

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton