Catalog Number

-

Brand Name

DK50 DS

Version/Model Number

ADV KOL MD 230V/50Hz 3,5bar NO

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

K091871

Product Code

BTI

Product Code Name

Compressor, Air, Portable

Public Device Record Key

25a0d5e4-6e55-4013-9747-46563077e68a

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

May 26, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-