Catalog Number

-

Brand Name

Secret RF Main Unit

Version/Model Number

MTR 2.0 Main Unit

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K170325

Product Code

OUH

Product Code Name

Skin Resurfacing Rf Applicator

Public Device Record Key

d954cc13-1af2-4e0c-954f-c23220bac18a

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

August 11, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-