Catalog Number

1005

Brand Name

OSOM Ultra Flu A&B Controls 5 Test

Version/Model Number

1005

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"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

GNX

Product Code Name

ANTIGENS, CF (INCLUDING CF CONTROL), INFLUENZA VIRUS A, B, C

Public Device Record Key

23b7d9a3-0c47-475a-9724-d28ffd4033f1

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

January 10, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-