Catalog Number

M490445

Brand Name

Percutaneous Introducer

Version/Model Number

M490445

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 03, 2019

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

K780126,K780126

Product Code

DRE

Product Code Name

Dilator, Vessel, For Percutaneous Catheterization

Public Device Record Key

a140bc21-6a3e-4c94-9dca-8c1317b20af5

Public Version Date

June 07, 2019

Public Version Number

5

DI Record Publish Date

September 21, 2016

Package DI Number

20886333216479

Quantity per Package

10

Contains DI Package

00886333216475

Package Discontinue Date

June 03, 2019

Package Status

Not in Commercial Distribution

Package Type

Box