Catalog Number

-

Brand Name

Trophy Skin

Version/Model Number

REJUVATONEMD

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

K152199

Product Code

NFO

Product Code Name

Stimulator, Transcutaneous Electrical, Aesthetic Purposes

Public Device Record Key

b0f50c58-ec18-41f5-a8d4-a98d9f3a2ab7

Public Version Date

February 10, 2020

Public Version Number

1

DI Record Publish Date

January 31, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-