Duns Number:329769991
Device Description: Cart Vyntus 3.0 230V
Catalog Number
V-859210
Brand Name
Vyntus
Version/Model Number
V-859210
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
July 29, 2020
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)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K150810
Product Code
BZC
Product Code Name
Calculator, Pulmonary Function Data
Public Device Record Key
47169e3e-97e7-49fe-a0a1-b123d0e7ebf5
Public Version Date
March 16, 2021
Public Version Number
4
DI Record Publish Date
July 31, 2018
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 | 76 |
2 | A medical device with a moderate to high risk that requires special controls. | 416 |