Catalog Number

-

Brand Name

McKesson

Version/Model Number

14-6N56C

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"

Yes

For Single-Use

Yes

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

LZA

Product Code Name

Polymer Patient Examination Glove

Public Device Record Key

0472cfc0-3082-4dba-85e3-45bbf3388701

Public Version Date

June 19, 2020

Public Version Number

2

DI Record Publish Date

August 30, 2019

Package DI Number

00612479247901

Quantity per Package

10

Contains DI Package

00612479247895

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case