Catalog Number

101

Brand Name

CorPath Interventional Cockpit

Version/Model Number

101

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

-

Product Code

IWX

Product Code Name

Barrier, Control Panel, X-Ray, Movable

Public Device Record Key

dcf49c0c-7467-4df6-a986-5192bea130a7

Public Version Date

October 19, 2022

Public Version Number

5

DI Record Publish Date

November 16, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-