Catalog Number

-

Brand Name

e-motion®

Version/Model Number

M15

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K003449

Product Code

ITI

Product Code Name

Wheelchair, Powered

Public Device Record Key

b94e5acb-e2b3-4535-9eaa-6b09a18ac0c2

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

April 27, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-