Duns Number:460060916
Device Description: Radiofrequency devices. Electrosurgical cutting and coagulation device and accessories
Catalog Number
ACT228
Brand Name
INDIBA ACTIV - ACTIV 801
Version/Model Number
ACT228
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
Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K161458
Product Code
PBX
Product Code Name
Massager, vacuum, radio frequency induced heat
Public Device Record Key
8b063376-d171-476d-8080-eed5c26a6cd7
Public Version Date
March 11, 2019
Public Version Number
1
DI Record Publish Date
February 22, 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. | 12 |