Catalog Number

-

Brand Name

AC Adapter for NE-C30

Version/Model Number

C30AC

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K060811,K060811

Product Code

CAF

Product Code Name

Nebulizer (Direct Patient Interface)

Public Device Record Key

778a96fc-fb39-45aa-8e42-abf184fd4738

Public Version Date

July 22, 2021

Public Version Number

4

DI Record Publish Date

September 16, 2016

Package DI Number

10073796330139

Quantity per Package

20

Contains DI Package

00073796330132

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case