Catalog Number

F900

Brand Name

RMS Precision Flow Rate TubingTM

Version/Model Number

F900

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

Yes

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

K933652,K933652

Product Code

FRN

Product Code Name

Pump, infusion

Public Device Record Key

c58e203f-390b-4952-bbb2-246ebcb6b039

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

August 19, 2016

Package DI Number

10659443000206

Quantity per Package

50

Contains DI Package

00659443000209

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton