Catalog Number

-

Brand Name

Enteral Feeding

Version/Model Number

ENF001

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

August 14, 2018

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K895367,K895367

Product Code

FPA

Product Code Name

Set, Administration, Intravascular

Public Device Record Key

21510b5e-842b-4964-9ab1-1ba021438b3d

Public Version Date

August 16, 2018

Public Version Number

4

DI Record Publish Date

September 22, 2016

Package DI Number

20020451100115

Quantity per Package

100

Contains DI Package

00020451100111

Package Discontinue Date

August 14, 2018

Package Status

Not in Commercial Distribution

Package Type

-