Catalog Number

-

Brand Name

VIVE

Version/Model Number

LVA1099GRY

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

-

Product Code

KNO

Product Code Name

Accessories, Wheelchair

Public Device Record Key

249c9d13-f18e-4fae-bc3a-28d686f2d512

Public Version Date

April 21, 2021

Public Version Number

3

DI Record Publish Date

March 24, 2019

Package DI Number

10818323025016

Quantity per Package

20

Contains DI Package

00818323025019

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case