Catalog Number

-

Brand Name

Shop Rite Pregnancy Test

Version/Model Number

FPPL

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

March 04, 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"

-

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

3d05a8ed-72e9-4798-b251-46b4085bc805

Public Version Date

March 05, 2019

Public Version Number

4

DI Record Publish Date

June 30, 2016

Package DI Number

10041190216694

Quantity per Package

24

Contains DI Package

00041190216697

Package Discontinue Date

March 04, 2019

Package Status

Not in Commercial Distribution

Package Type

Shipping case