Catalog Number

-

Brand Name

IB Rad Tech

Version/Model Number

1.2

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

November 16, 2017

Issuing Agency

In HIBCC

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

K123302

Product Code

LLZ

Product Code Name

System, Image Processing, Radiological

Public Device Record Key

ab10dd5c-7a55-4e69-8c99-d2bcfed10677

Public Version Date

October 07, 2019

Public Version Number

5

DI Record Publish Date

September 23, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-