Duns Number:056332380
Catalog Number
-
Brand Name
Aerochamber Plus® Z STAT®
Version/Model Number
aVHC, Small Mask, cs/10
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
K052332,K052332
Product Code
NVP
Product Code Name
Holding Chambers, Direct Patient Interface
Public Device Record Key
f8083b85-c142-4b1e-983b-68a3aa50e787
Public Version Date
September 09, 2021
Public Version Number
4
DI Record Publish Date
September 22, 2016
Package DI Number
50604351887102
Quantity per Package
10
Contains DI Package
00604351887107
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 | 7 |
2 | A medical device with a moderate to high risk that requires special controls. | 39 |