Catalog Number

-

Brand Name

Drive

Version/Model Number

AZ0060

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

-

Product Code

KNO

Product Code Name

ACCESSORIES, WHEELCHAIR

Public Device Record Key

148d4451-e74c-4ac6-b7e1-2dac065942a2

Public Version Date

July 03, 2019

Public Version Number

1

DI Record Publish Date

June 25, 2019

Package DI Number

50822383274794

Quantity per Package

25

Contains DI Package

00822383274799

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-