Catalog Number

ID-THC

Brand Name

Identify Diagnostics Drug Test Cards

Version/Model Number

ID-THC

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LDJ

Product Code Name

Enzyme Immunoassay, Cannabinoids

Public Device Record Key

62e8564b-f8bc-409b-bc56-9c13adb49016

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

October 08, 2016

Package DI Number

20850721007369

Quantity per Package

40

Contains DI Package

10850721007362

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case