Duns Number:197934250
Device Description: For the calibration of the K-ASSAY® RF (Ver.2) assay
Catalog Number
KAI-231C
Brand Name
K-ASSAY® RF Calibrator (Ver.2)
Version/Model Number
KAI-231C
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
K192727
Product Code
JIS
Product Code Name
Calibrator, Primary
Public Device Record Key
673e21a5-15bc-4ca1-beee-10cb4f26dd32
Public Version Date
November 11, 2020
Public Version Number
1
DI Record Publish Date
November 03, 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 | 49 |
2 | A medical device with a moderate to high risk that requires special controls. | 66 |