Duns Number:966390890
Device Description: Precision Xtra Blood Glucose Test Strips
Catalog Number
99878
Brand Name
Precision Xtra
Version/Model Number
99878
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
K051213,K051213,K051213
Product Code
LFR
Product Code Name
Glucose dehydrogenase, glucose
Public Device Record Key
84b6fe9c-144b-4fa5-ada6-f40656a9375f
Public Version Date
December 11, 2019
Public Version Number
5
DI Record Publish Date
July 22, 2016
Package DI Number
30093815998786
Quantity per Package
6
Contains DI Package
00093815998785
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 |