Catalog Number

-

Brand Name

Vios

Version/Model Number

310F35-NDP

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

K092918,K092918

Product Code

CAF

Product Code Name

Nebulizer (Direct Patient Interface)

Public Device Record Key

6023b3ba-74b5-4441-afd5-63aa60633c34

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 27, 2016

Package DI Number

00744229311089

Quantity per Package

6

Contains DI Package

00744229310617

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

carton