Catalog Number

QT80F-CE

Brand Name

QuickTox Drug Screen Dipcard

Version/Model Number

QT80F-CE

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 09, 2020

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

K022355,K082508

Product Code

DIO

Product Code Name

Enzyme Immunoassay, Cocaine And Cocaine Metabolites

Public Device Record Key

16a0318a-266c-4070-8d87-a60dada74957

Public Version Date

June 10, 2022

Public Version Number

6

DI Record Publish Date

September 19, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-