Duns Number:080651010
Device Description: Marijuana THC Single Drug Test Dip Card
Catalog Number
-
Brand Name
PreKnow
Version/Model Number
21115061010308
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)
Yes
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K153050,K153050
Product Code
LDJ
Product Code Name
Enzyme Immunoassay, Cannabinoids
Public Device Record Key
70072cd2-9c3e-43d5-ac03-eeafe396faea
Public Version Date
June 10, 2022
Public Version Number
3
DI Record Publish Date
August 02, 2018
Package DI Number
00857275007384
Quantity per Package
25
Contains DI Package
00857275007506
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 1 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 12 |