Catalog Number

MTSBRT014

Brand Name

Transfer Guide

Version/Model Number

MTSBRT014

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

February 08, 2020

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

6d4a0625-1c3d-4c01-9623-0455e0523727

Public Version Date

February 10, 2020

Public Version Number

6

DI Record Publish Date

August 02, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-