Catalog Number

AI-07138

Brand Name

ARROW

Version/Model Number

IPN917241

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)

Yes

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

K892530,K892530

Product Code

DYG

Product Code Name

CATHETER, FLOW DIRECTED

Public Device Record Key

35256493-cce1-4dab-8519-ed5c85fc0319

Public Version Date

September 16, 2022

Public Version Number

2

DI Record Publish Date

August 12, 2021

Package DI Number

20801902180838

Quantity per Package

5

Contains DI Package

10801902180831

Package Discontinue Date

September 13, 2022

Package Status

Not in Commercial Distribution

Package Type

Case