Duns Number:315786293
Device Description: Alinity i CA 15-3 Reagent Kit 1000 Tests
Catalog Number
08P5130
Brand Name
Alinity
Version/Model Number
08P5130
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
K042732
Product Code
MOI
Product Code Name
SYSTEM, TEST, IMMUNOLOGICAL, ANTIGEN, TUMOR
Public Device Record Key
89b304b4-9f42-455d-960c-8ac100c9f6c6
Public Version Date
April 05, 2021
Public Version Number
3
DI Record Publish Date
December 31, 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 | 347 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 185 |
| 3 | A medical device with high risk that requires premarket approval | 13 |