Duns Number:004321519
Device Description: SURE-VUE CRP 500 TESTS/PK
Catalog Number
23046389
Brand Name
Sure-Vue
Version/Model Number
T3018-7549
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
K896272,K896272
Product Code
DCN
Product Code Name
SYSTEM, TEST, C-REACTIVE PROTEIN
Public Device Record Key
cc052275-5e8c-461c-a696-a1415e6e2dc3
Public Version Date
June 10, 2022
Public Version Number
4
DI Record Publish Date
October 27, 2017
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 | 129 |
2 | A medical device with a moderate to high risk that requires special controls. | 36 |