Catalog Number

HT-LT2501C

Brand Name

Sinton Medical Products

Version/Model Number

600101-1

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

d3175119-1717-4abb-b9c7-679f8a88de0f

Public Version Date

April 03, 2020

Public Version Number

3

DI Record Publish Date

August 15, 2018

Package DI Number

26938327902777

Quantity per Package

2

Contains DI Package

16938327902770

Package Discontinue Date

December 31, 9999

Package Status

In Commercial Distribution

Package Type

Carton