Catalog Number

-

Brand Name

NA

Version/Model Number

170730

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 06, 2016

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

K121448,K132816

Product Code

MUJ

Product Code Name

System,planning,radiation therapy treatment

Public Device Record Key

ac0913fe-63de-439b-8e12-c4dfc41a454b

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

October 20, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-