Catalog Number

-

Brand Name

VSI StraitSet™ micro-introducer kit

Version/Model Number

7960

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

K071330,K071330

Product Code

DRE

Product Code Name

Dilator, Vessel, For Percutaneous Catheterization

Public Device Record Key

e1263b85-afa0-4255-a585-3ce623fd4209

Public Version Date

June 07, 2019

Public Version Number

2

DI Record Publish Date

August 09, 2018

Package DI Number

M20679601

Quantity per Package

10

Contains DI Package

M20679600

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box