Catalog Number

-

Brand Name

CIRRUS 2 NEBULISER

Version/Model Number

1402000

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

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

Yes

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

-

FDA Premarket Submission

K911422,K911422

Product Code

CAF

Product Code Name

Nebulizer (Direct Patient Interface)

Public Device Record Key

bd3c9ef9-20c8-4288-9ddc-4585f2ca2ea5

Public Version Date

July 20, 2022

Public Version Number

1

DI Record Publish Date

July 12, 2022

Package DI Number

05030267083152

Quantity per Package

75

Contains DI Package

05030267083145

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-