Duns Number:966390890
Device Description: Precision Xceed Pro Blood ß-Ketone Test Strips
Catalog Number
70935
Brand Name
Precision Xceed Pro
Version/Model Number
70935
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
K080960,K080960,K080960
Product Code
JIN
Product Code Name
NITROPRUSSIDE, KETONES (URINARY, NON-QUANT.)
Public Device Record Key
b5710df3-4aaa-48f2-9d00-666e99978049
Public Version Date
December 11, 2019
Public Version Number
5
DI Record Publish Date
July 22, 2016
Package DI Number
35021791709350
Quantity per Package
12
Contains DI Package
00093815709350
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 13 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 19 |
| 3 | A medical device with high risk that requires premarket approval | 2 |