Duns Number:962385787
Device Description: LDLD (LDL Cholesterol Direct) w/ cal 2 x 200 tests
Catalog Number
CC667
Brand Name
CAROLINA LIQUID CHEMISTRIES CORP.® LDL DIRECT REAGENT CC667
Version/Model Number
CC667
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 27, 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
Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
LBR
Product Code Name
LDL & VLDL PRECIPITATION, HDL
Public Device Record Key
cd510ead-9dd9-40db-b56d-646bdebe52eb
Public Version Date
September 27, 2018
Public Version Number
1
DI Record Publish Date
August 27, 2018
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 | 144 |
2 | A medical device with a moderate to high risk that requires special controls. | 183 |
U | Unclassified | 7 |