Catalog Number

GX240-CL-BK

Brand Name

RadiForce®

Version/Model Number

GX240

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

K120407,K120407

Product Code

LLZ

Product Code Name

System, Image Processing, Radiological

Public Device Record Key

5d1114b3-0530-470a-a270-d36dd20ad6ae

Public Version Date

October 24, 2022

Public Version Number

2

DI Record Publish Date

July 30, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-