Catalog Number

K Pump

Brand Name

MD Resource

Version/Model Number

K Pump

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K012044

Product Code

FRN

Product Code Name

Pump, Infusion

Public Device Record Key

e140c190-c231-47c3-b898-4b0a3e6f7633

Public Version Date

July 04, 2022

Public Version Number

5

DI Record Publish Date

September 08, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-