Catalog Number

-

Brand Name

7E Wellness

Version/Model Number

MYOLIFT ULTRA

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

K112351

Product Code

NFO

Product Code Name

Stimulator, Transcutaneous Electrical, Aesthetic Purposes

Public Device Record Key

fa7fc974-ea2f-481d-b5ee-9c8b85e49070

Public Version Date

February 19, 2021

Public Version Number

7

DI Record Publish Date

September 19, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-