Catalog Number

-

Brand Name

McKesson

Version/Model Number

37-6503

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

-

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

K083042,K083042

Product Code

FRO

Product Code Name

Dressing, Wound, Drug

Public Device Record Key

4a3be24a-5168-400a-afd3-8b5f9a55c88c

Public Version Date

February 21, 2022

Public Version Number

2

DI Record Publish Date

March 09, 2020

Package DI Number

00612479228429

Quantity per Package

12

Contains DI Package

00612479228412

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case