Duns Number:163610020
Device Description: TCA Single Panel Dip Test Card
Catalog Number
U-TCA-114
Brand Name
UCP Home Drug Screening Test Cards
Version/Model Number
U-TCA-114
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
K050540,K061457,K130463,K050540,K061457,K130463,K050540,K061457,K130463
Product Code
LFG
Product Code Name
Radioimmunoassay, Tricyclic Antidepressant Drugs
Public Device Record Key
f1627021-6c65-4fa9-83e2-fc1fbd9cd147
Public Version Date
June 10, 2022
Public Version Number
4
DI Record Publish Date
August 30, 2016
Package DI Number
20817038020023
Quantity per Package
40
Contains DI Package
10817038020026
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
case
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 2 |