Catalog Number

801801B

Brand Name

LF

Version/Model Number

200103-C

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

December 31, 9999

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"

-

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

K151960,K151960,K151960

Product Code

DXT

Product Code Name

Injector And Syringe, Angiographic

Public Device Record Key

c7b63027-b0a9-409e-99fd-4f630c10d130

Public Version Date

May 31, 2021

Public Version Number

2

DI Record Publish Date

March 05, 2021

Package DI Number

16938327906075

Quantity per Package

10

Contains DI Package

06938327906078

Package Discontinue Date

December 31, 9999

Package Status

In Commercial Distribution

Package Type

box