Catalog Number

-

Brand Name

KY UltraGel Personal Lubricant

Version/Model Number

Personal Lubricant

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

K020827,K192982,K020827,K192982,K020827,K192982

Product Code

NUC

Product Code Name

Lubricant, personal

Public Device Record Key

a33143b5-6427-4d04-a10a-efbbe8d6a5d9

Public Version Date

April 05, 2022

Public Version Number

6

DI Record Publish Date

September 20, 2016

Package DI Number

10067981087359

Quantity per Package

6

Contains DI Package

00067981087352

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton