Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

81085

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

February 22, 2022

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

LRS

Product Code Name

I.V. start kit

Public Device Record Key

768a4a0a-ef6e-4d22-b9e1-d9ec7d1ea0d2

Public Version Date

February 23, 2022

Public Version Number

3

DI Record Publish Date

July 16, 2020

Package DI Number

20809160287962

Quantity per Package

20

Contains DI Package

10809160287965

Package Discontinue Date

February 22, 2022

Package Status

Not in Commercial Distribution

Package Type

-