Catalog Number

-

Brand Name

CADD

Version/Model Number

21-2112-0402-78

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K170982

Product Code

FPA

Product Code Name

Set, administration, intravascular

Public Device Record Key

b80966a0-1fa3-4177-acc5-717fabad6294

Public Version Date

July 04, 2022

Public Version Number

3

DI Record Publish Date

December 05, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-