Catalog Number

302

Brand Name

CorPath GRX Extended Reach Arm

Version/Model Number

302

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

Product Code

DXX

Product Code Name

System, Catheter Control, Steerable

Public Device Record Key

7c086c14-b4a1-4d3e-93b1-a405055c2e24

Public Version Date

October 19, 2022

Public Version Number

6

DI Record Publish Date

January 20, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-