Duns Number:164880598
Device Description: The ARK™ Topiramate Control consists of a three-level set used for quality control of the The ARK™ Topiramate Control consists of a three-level set used for quality control of the ARK™ Topiramate Assay.
Catalog Number
5015-0003-00
Brand Name
ARK™ Topiramate Control
Version/Model Number
5015-0003-00
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
K083799
Product Code
LAS
Product Code Name
Drug Specific Control Materials
Public Device Record Key
0d6141b7-f4fa-429a-adfd-428d1b13ef19
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 24, 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 | 30 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 86 |
| U | Unclassified | 4 |