Catalog Number

-

Brand Name

Seracult Plus Fecal Occult Blood Test Developer

Version/Model Number

37701500

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K834297,K834297

Product Code

KHE

Product Code Name

Reagent, Occult Blood

Public Device Record Key

252a1564-b1b8-46c9-b527-650f57e0d675

Public Version Date

December 21, 2020

Public Version Number

2

DI Record Publish Date

May 20, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-