Catalog Number

-

Brand Name

AeroChamber Plus® Flow-Vu®

Version/Model Number

aVHC, Medium Mask Demo, Allergan, Single

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

K112010

Product Code

NVP

Product Code Name

Holding Chambers, Direct Patient Interface

Public Device Record Key

1f2d9ffd-ac8c-42c4-a26e-07ecd5e0d14f

Public Version Date

September 09, 2021

Public Version Number

4

DI Record Publish Date

September 30, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-