Catalog Number

AU-0984SC

Brand Name

Austin Medical

Version/Model Number

AU-0984SC

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)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K061422,K061422

Product Code

KKX

Product Code Name

Drape, Surgical

Public Device Record Key

0252c27d-a581-4557-8a78-de210075f45e

Public Version Date

December 22, 2021

Public Version Number

6

DI Record Publish Date

December 09, 2016

Package DI Number

00866001000315

Quantity per Package

10

Contains DI Package

00866001000308

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case