Catalog Number

-

Brand Name

6000A

Version/Model Number

6000A

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

Yes

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

K090738,K090738,K090738,K090738,K090738

Product Code

CAH

Product Code Name

Filter, Bacterial, Breathing-Circuit

Public Device Record Key

f2eb4913-80e4-48c0-91f9-919778a3b127

Public Version Date

December 22, 2021

Public Version Number

2

DI Record Publish Date

January 15, 2020

Package DI Number

40850015328044

Quantity per Package

450

Contains DI Package

00850015328046

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-