Catalog Number

-

Brand Name

MC 300® Reusable Nebulizer

Version/Model Number

105552

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

K173825,K173825,K173825,K173825

Product Code

CAF

Product Code Name

Nebulizer (Direct Patient Interface)

Public Device Record Key

aa070639-4969-4e07-adb2-9162b0252c11

Public Version Date

February 26, 2020

Public Version Number

1

DI Record Publish Date

February 18, 2020

Package DI Number

20762860055524

Quantity per Package

50

Contains DI Package

00762860055520

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-