Duns Number:045623154
Device Description: For the quantitative enzymatic determination of creatinine in serum and urine. For In Vitr For the quantitative enzymatic determination of creatinine in serum and urine. For In Vitro Diagnostic Use Only.
Catalog Number
12-C7548-162
Brand Name
Creatinine Enzymatic
Version/Model Number
12-C7548-162
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K050283
Product Code
JFY
Product Code Name
Enzymatic Method, Creatinine
Public Device Record Key
66a6d5bc-028d-4506-b2af-33f4c27ea1dd
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
August 31, 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 | 217 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 455 |
| U | Unclassified | 2 |