Catalog Number

-

Brand Name

Mckesson

Version/Model Number

14-1380

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)

Yes

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

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

K013554,K013554,K013554

Product Code

LYY

Product Code Name

Latex Patient Examination Glove

Public Device Record Key

67cef5c6-3585-4dfe-ae01-772b2c0fc9b7

Public Version Date

May 07, 2021

Public Version Number

2

DI Record Publish Date

August 04, 2020

Package DI Number

00612479188211

Quantity per Package

10

Contains DI Package

00612479188204

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case