Duns Number:227530649
Device Description: A glucose test system is a device intended for the quantitative in vitro determination of A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine
Catalog Number
GL3981
Brand Name
GLUC-PAP
Version/Model Number
GL3981
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K003346
Product Code
CGA
Product Code Name
Glucose Oxidase, Glucose
Public Device Record Key
4f84b3c6-7b88-465a-98de-2288d7ffd58c
Public Version Date
June 28, 2021
Public Version Number
3
DI Record Publish Date
September 16, 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 | 305 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 258 |