Catalog Number

4155017P

Brand Name

NUTRI-CATH

Version/Model Number

Polyurethane

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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"

Yes

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

K861090,K861090

Product Code

KNT

Product Code Name

Tubes, Gastrointestinal (And Accessories)

Public Device Record Key

1727e25b-f197-4253-a0a9-1e327cd4ddd2

Public Version Date

December 19, 2019

Public Version Number

4

DI Record Publish Date

September 23, 2016

Package DI Number

H6714155017P1

Quantity per Package

10

Contains DI Package

H6714155017P0

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box