Catalog Number

MTT-010-LP

Brand Name

Moore Tube Low-Profile Inner Cannula

Version/Model Number

MTT-010-LP

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

MRI safety Status

MR Safe

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

-

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

K962240,K962240

Product Code

BTO

Product Code Name

Tube, Tracheostomy (W/Wo Connector)

Public Device Record Key

e446b913-4571-4063-bec6-ecf3f588cb53

Public Version Date

August 30, 2022

Public Version Number

4

DI Record Publish Date

September 20, 2015

Package DI Number

EBESMTT010LP1

Quantity per Package

2

Contains DI Package

EBESMTT010LP0

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton