Catalog Number

HS1500AS

Brand Name

Hays Inc.

Version/Model Number

HS1500AS

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

K101689,K101689,K101689

Product Code

KKX

Product Code Name

Drape, Surgical

Public Device Record Key

5f3ce94f-fe2d-4f33-b4f5-e8aae9a83b8e

Public Version Date

June 10, 2020

Public Version Number

1

DI Record Publish Date

June 02, 2020

Package DI Number

00860003700839

Quantity per Package

20

Contains DI Package

00860003700822

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

inner case