Catalog Number

-

Brand Name

HONEYWELL

Version/Model Number

HC888T

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

-

Product Code

KFZ

Product Code Name

Humidifier, Non-Direct Patient Interface (Home-Use)

Public Device Record Key

17b5fe18-a6d3-4999-972b-09cb006f1fe0

Public Version Date

May 27, 2020

Public Version Number

2

DI Record Publish Date

August 31, 2018

Package DI Number

10092926108882

Quantity per Package

6

Contains DI Package

00092926108885

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE