Catalog Number

-

Brand Name

Neutrogena

Version/Model Number

00070501101247

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 22, 2020

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

-

Product Code

OLP

Product Code Name

Over-the-counter powered light based laser for acne

Public Device Record Key

b6053cff-a2ad-4de5-9b2c-f0240ad22587

Public Version Date

June 23, 2020

Public Version Number

4

DI Record Publish Date

September 30, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-