Duns Number:080278407
Device Description: 25 tests kit;14-Panel T-Cup 3-AD; COC/THC/OPI/BZO/MET/TCA/OXY/BUP/BAR/MTD/AMP/MDMA/PCP/PPX 25 tests kit;14-Panel T-Cup 3-AD; COC/THC/OPI/BZO/MET/TCA/OXY/BUP/BAR/MTD/AMP/MDMA/PCP/PPX)OX/SG/PH
Catalog Number
-
Brand Name
Easy@Home Multi-Drug Test Cup (25 tests kit)
Version/Model Number
ECDOA-1144A3
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)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K133968,K133968,K133968
Product Code
CAF
Product Code Name
Nebulizer (Direct Patient Interface)
Public Device Record Key
02a064b6-15ec-4a97-b7ae-0cb4ce0d6255
Public Version Date
July 25, 2022
Public Version Number
9
DI Record Publish Date
September 15, 2016
Package DI Number
10850253007601
Quantity per Package
4
Contains DI Package
00850253007604
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 | 4 |
2 | A medical device with a moderate to high risk that requires special controls. | 47 |