Catalog Number

-

Brand Name

Drive

Version/Model Number

93677 AQUA

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

KMN

Product Code Name

CHAIR AND TABLE, MEDICAL

Public Device Record Key

bdb47dbf-dc11-43a2-800e-9afbd2fea4ad

Public Version Date

July 03, 2019

Public Version Number

1

DI Record Publish Date

June 25, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-