Duns Number:785966607
Device Description: Detection of Syphilis, 10 well, TDH
Catalog Number
NC-9005000-10T
Brand Name
ASI RPR Card Test for Syphilis
Version/Model Number
NC-9005000-10T
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K851504
Product Code
GMP
Product Code Name
Antisera, Control For Nontreponemal Tests
Public Device Record Key
8fd39742-2b19-4f0c-8e8a-80386c801373
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
July 08, 2016
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 | 25 |
2 | A medical device with a moderate to high risk that requires special controls. | 115 |