Catalog Number

AI-07134

Brand Name

ARROW

Version/Model Number

IPN917232

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

4f011402-215a-49b3-b0ef-3f24b01e0cd2

Public Version Date

August 19, 2021

Public Version Number

1

DI Record Publish Date

August 11, 2021

Package DI Number

20801902180753

Quantity per Package

5

Contains DI Package

10801902180756

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case