Catalog Number

-

Brand Name

Ethos™ Treatment Planning

Version/Model Number

1.1

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K212294

Product Code

MUJ

Product Code Name

System, planning, radiation therapy treatment

Public Device Record Key

fb686a0b-9555-4a37-a517-323868fa8ccd

Public Version Date

September 13, 2021

Public Version Number

1

DI Record Publish Date

September 03, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-