Catalog Number

CA-300

Brand Name

ICU Medical

Version/Model Number

CA-300

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

-

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

-

FDA Premarket Submission

K970855,K970855

Product Code

FPA

Product Code Name

Set, administration, intravascular

Public Device Record Key

da5fae60-87b5-4248-80b4-54e6819166a6

Public Version Date

September 01, 2021

Public Version Number

1

DI Record Publish Date

August 24, 2021

Package DI Number

10887709037110

Quantity per Package

50

Contains DI Package

00887709037113

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS