Duns Number:008254708
Device Description: The Access CK-MB Calibrators are intended to calibrate the Access CK-MB assay for the quan The Access CK-MB Calibrators are intended to calibrate the Access CK-MB assay for the quantitative determination of CK-MB levels in human serum and plasma using the Access Immunoassay Systems.
Catalog Number
386372
Brand Name
Access CK-MB Calibrators
Version/Model Number
386372
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
-
Product Code
JIS
Product Code Name
Calibrator, Primary
Public Device Record Key
01bc4751-3560-4c5e-80e9-8adeaf608900
Public Version Date
April 09, 2018
Public Version Number
3
DI Record Publish Date
September 09, 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 | 319 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 503 |
| 3 | A medical device with high risk that requires premarket approval | 9 |
| U | Unclassified | 1 |