Catalog Number

MTIL6151

Brand Name

Reference Device for TrueBeam

Version/Model Number

MTIL6151

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

K973842

Product Code

IXQ

Product Code Name

Table, radiographic, stationary top

Public Device Record Key

1c3d9ba6-3fdd-4b5a-adc7-c5617ff01ce8

Public Version Date

March 27, 2020

Public Version Number

3

DI Record Publish Date

August 22, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-