Catalog Number

-

Brand Name

Nu Skin Facial Spa

Version/Model Number

90025509

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

K122711

Product Code

NFO

Product Code Name

Stimulator, transcutaneous electrical, aesthetic purposes

Public Device Record Key

e4c4ee2d-8b21-4ce2-86cb-6a95f2cb1d8c

Public Version Date

October 23, 2019

Public Version Number

5

DI Record Publish Date

September 28, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-