Catalog Number

01VB0103

Brand Name

N/A

Version/Model Number

Nebuliser Tube System

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K090730

Product Code

CAF

Product Code Name

Nebulizer (Direct Patient Interface)

Public Device Record Key

17c4da77-f2c1-4f83-9880-239cbd7c7e36

Public Version Date

June 10, 2022

Public Version Number

7

DI Record Publish Date

June 27, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-