Duns Number:227530649
Device Description: The device is intended for use in the quality control of CK-MB assays on clinical chemist The device is intended for use in the quality control of CK-MB assays on clinical chemistry systems.
Catalog Number
CK1212
Brand Name
CK-MB CONTROL
Version/Model Number
CK1212
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
K951223
Product Code
CGS
Product Code Name
Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes
Public Device Record Key
583c04ef-927a-49e2-9548-dfb3b7063cf0
Public Version Date
July 06, 2018
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 |