Duns Number:062312574
Device Description: A convenience kit consisting of 1 CVS One Step Pregnancy Test, 1 CVS Early Result Pregnanc A convenience kit consisting of 1 CVS One Step Pregnancy Test, 1 CVS Early Result Pregnancy Test and 1 CVS Digital Yes+ No- Pregnancy Test
Catalog Number
-
Brand Name
CVS Health
Version/Model Number
Triple Test Pregnancy Test Kit
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
K042280,K060128,K042280,K060128
Product Code
LCX
Product Code Name
Kit, Test, Pregnancy, Hcg, Over The Counter
Public Device Record Key
0da1b844-86c4-4d43-9da9-e6759650955a
Public Version Date
March 09, 2020
Public Version Number
1
DI Record Publish Date
February 28, 2020
Package DI Number
10050428624040
Quantity per Package
24
Contains DI Package
00050428624043
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Shipping Case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 82 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 139 |
| U | Unclassified | 23 |