Catalog Number

AI-07121

Brand Name

ARROW

Version/Model Number

IPN923524

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

c86ad931-5892-47c4-81ae-3989113a7d0f

Public Version Date

March 22, 2022

Public Version Number

1

DI Record Publish Date

March 14, 2022

Package DI Number

20801902206712

Quantity per Package

5

Contains DI Package

10801902206715

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case