Catalog Number

301

Brand Name

CorPath GRX Control Console

Version/Model Number

301

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)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

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

K160121,K173288,K202275

Product Code

DXX

Product Code Name

System, Catheter Control, Steerable

Public Device Record Key

321a92e7-cf38-457c-b0c4-d559f6c29237

Public Version Date

October 19, 2022

Public Version Number

8

DI Record Publish Date

January 20, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-