Duns Number:829221139
Device Description: Patient application for Android
Catalog Number
-
Brand Name
Kintinuum™
Version/Model Number
SW-0042
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
April 01, 2021
Issuing Agency
In HIBCC
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"
Yes
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
-
Product Code
ISD
Product Code Name
Exerciser, Measuring
Public Device Record Key
a76ee68b-6b92-40e3-b075-4f248870f7cd
Public Version Date
April 02, 2021
Public Version Number
3
DI Record Publish Date
February 01, 2019
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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 28 |