Duns Number:197934250
Device Description: For the calibration of the K-ASSAY® Fructosamine assay.
Catalog Number
KAI-048C
Brand Name
K-ASSAY® Fructosamine Calibrator
Version/Model Number
KAI-048C
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 28, 2018
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
LCP
Product Code Name
Assay, Glycosylated Hemoglobin
Public Device Record Key
c1fd9ee3-51ae-4e5e-8ba6-8c99a58f18c8
Public Version Date
January 01, 2019
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 | 49 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 66 |