Catalog Number

-

Brand Name

dpl®

Version/Model Number

DPLNUVEAA

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

-

Product Code

OHS

Product Code Name

Light Based Over The Counter Wrinkle Reduction

Public Device Record Key

f3ee5804-2cd5-44ec-8b38-7275d0fa4f5f

Public Version Date

July 07, 2020

Public Version Number

3

DI Record Publish Date

September 20, 2016

Package DI Number

B347DPLNUVEAA1

Quantity per Package

20

Contains DI Package

B347DPLNUVEAA0

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-