Catalog Number

6-87168

Brand Name

Moss

Version/Model Number

6-87168

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K984629

Product Code

BSS

Product Code Name

TUBE, NASOGASTRIC

Public Device Record Key

4eba7f7e-a47a-4507-b718-3b4549758575

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

October 04, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-