Duns Number:690598875
Device Description: In-Vitro Diagnostic Use
Catalog Number
997-72591
Brand Name
L-Type HDL-C Reagent 1
Version/Model Number
997-72591
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
K963847,K963847,K963847
Product Code
LBR
Product Code Name
Ldl & Vldl Precipitation, Hdl
Public Device Record Key
88122cab-49c1-4f9a-a92d-5b2a365115b5
Public Version Date
March 08, 2022
Public Version Number
3
DI Record Publish Date
October 23, 2020
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 |