Duns Number:092673953
Catalog Number
-
Brand Name
Vibralung Battery Charger
Version/Model Number
9630
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"
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
K133057,K133057
Product Code
BYI
Product Code Name
Percussor, Powered-Electric
Public Device Record Key
b9012539-8826-4328-bd9d-d3d4a1e2ddc8
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
December 15, 2016
Package DI Number
10709078001533
Quantity per Package
1
Contains DI Package
00709078001536
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 746 |
2 | A medical device with a moderate to high risk that requires special controls. | 320 |