Duns Number:690598875
Device Description: In-Vitro Diagnostic Use
Catalog Number
990-28011
Brand Name
HDL-C/LDL-C Calibrator
Version/Model Number
990-28011
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
October 23, 2020
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
K001005,K001005
Product Code
JIS
Product Code Name
Calibrator, Primary
Public Device Record Key
d7632d9c-33a0-46b4-b87f-224d7286a0ff
Public Version Date
March 08, 2022
Public Version Number
6
DI Record Publish Date
December 07, 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 | 18 |
2 | A medical device with a moderate to high risk that requires special controls. | 22 |