Duns Number:006961700
Device Description: PLPL TARGET (UP&UP) DPS Early Result
Catalog Number
-
Brand Name
Up & Up
Version/Model Number
Early-Result Pregnancy Tests
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
April 19, 2021
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,K042280,K042280,K042280
Product Code
LCX
Product Code Name
Kit, Test, Pregnancy, Hcg, Over The Counter
Public Device Record Key
b7765266-e646-4960-9fa4-b9d2684e3421
Public Version Date
April 20, 2021
Public Version Number
2
DI Record Publish Date
April 24, 2020
Package DI Number
10751774733522
Quantity per Package
12
Contains DI Package
00751774733525
Package Discontinue Date
April 19, 2021
Package Status
Not 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 | 22 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 52 |
| U | Unclassified | 12 |