Duns Number:735575941
Device Description: Neuromuscular Electrical Stimulation Device
Catalog Number
1718
Brand Name
Revitive Circulation Booster
Version/Model Number
RIX
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)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K143207,K143207
Product Code
NGX
Product Code Name
Stimulator, Muscle, Powered, For Muscle Conditioning
Public Device Record Key
bacec4a1-0e63-4b47-9107-784dd0cd585f
Public Version Date
May 23, 2019
Public Version Number
3
DI Record Publish Date
April 23, 2018
Package DI Number
10858058005013
Quantity per Package
6
Contains DI Package
00858058005016
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Outer carton
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 11 |