Catalog Number

20112

Brand Name

QuickVue

Version/Model Number

20112

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

K102175

Product Code

JHI

Product Code Name

Visual, pregnancy hCG, prescription use

Public Device Record Key

1d969ee4-23d5-4cd0-8ca6-4d962c2f5e05

Public Version Date

January 09, 2019

Public Version Number

2

DI Record Publish Date

November 10, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-