Catalog Number

8624736

Brand Name

DRX-Compass X-ray System

Version/Model Number

DRX-Compass X-ray System

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

K201373

Product Code

KPR

Product Code Name

System, x-ray, stationary

Public Device Record Key

5763c12b-7fc4-419d-a820-8e89fdff1ca9

Public Version Date

July 21, 2021

Public Version Number

1

DI Record Publish Date

July 13, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-