Catalog Number

76092-ACM5202

Brand Name

Halyard

Version/Model Number

05202

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

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

KKX

Product Code Name

Drape, surgical

Public Device Record Key

a59e4906-df3b-461e-bc4e-177499ab519e

Public Version Date

December 22, 2021

Public Version Number

7

DI Record Publish Date

September 10, 2016

Package DI Number

30680651052026

Quantity per Package

15

Contains DI Package

10680651052022

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS