Catalog Number

-

Brand Name

Equate

Version/Model Number

One Step Pregnancy Test

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K042280,K042280,K042280

Product Code

LCX

Product Code Name

Kit, Test, Pregnancy, Hcg, Over The Counter

Public Device Record Key

bceecbe8-41f2-4ef0-82bc-ad02c9ba6766

Public Version Date

October 29, 2018

Public Version Number

1

DI Record Publish Date

September 28, 2018

Package DI Number

10681131240816

Quantity per Package

24

Contains DI Package

00681131240819

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Shipping case