Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

58252

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

February 26, 2020

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

Yes

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

-

FDA Premarket Submission

-

Product Code

FKG

Product Code Name

TRAY, START/STOP (INCLUDING CONTENTS), DIALYSIS

Public Device Record Key

f434d6a9-a53f-47f7-a758-d219ab0e2342

Public Version Date

February 27, 2020

Public Version Number

4

DI Record Publish Date

August 20, 2016

Package DI Number

20809160008246

Quantity per Package

20

Contains DI Package

10809160008249

Package Discontinue Date

February 26, 2020

Package Status

Not in Commercial Distribution

Package Type

-