Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

78877

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

February 11, 2019

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

c004df0c-e7ec-415f-9325-0693b5640b4b

Public Version Date

December 11, 2019

Public Version Number

3

DI Record Publish Date

November 19, 2018

Package DI Number

20809160219048

Quantity per Package

30

Contains DI Package

10809160219041

Package Discontinue Date

February 11, 2019

Package Status

Not in Commercial Distribution

Package Type

-