Catalog Number

-

Brand Name

Lunit INSIGHT CXR Triage

Version/Model Number

1.0

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

K211733

Product Code

QFM

Product Code Name

Radiological Computer-Assisted Prioritization Software For Lesions

Public Device Record Key

bb1af085-b6e5-434a-87c8-fb3b32af9c49

Public Version Date

October 28, 2022

Public Version Number

3

DI Record Publish Date

April 28, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-