Catalog Number

-

Brand Name

Drive

Version/Model Number

MQ5300

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

April 24, 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

-

Product Code

BTI

Product Code Name

Compressor, air, portable

Public Device Record Key

1ca03007-9c37-4c05-84d9-49703576e26e

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

September 16, 2016

Package DI Number

10822383579099

Quantity per Package

6

Contains DI Package

00822383579092

Package Discontinue Date

April 24, 2020

Package Status

Not in Commercial Distribution

Package Type

-