Duns Number:966390890
Device Description: Precision Xceed Pro Blood Glucose and ß-Ketone Monitoring System
Catalog Number
70900-05
Brand Name
Precision Xceed Pro
Version/Model Number
70900-05
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
-
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
Product Code
JIN
Product Code Name
NITROPRUSSIDE, KETONES (URINARY, NON-QUANT.)
Public Device Record Key
faeca891-4377-41c3-91cc-d2cb41a115a7
Public Version Date
December 11, 2019
Public Version Number
6
DI Record Publish Date
August 12, 2016
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| 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 |