Catalog Number

-

Brand Name

DIAGNOSTIC ULTRASOUND SYSTEM

Version/Model Number

TUS-AI900

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K161843

Product Code

ITX

Product Code Name

Transducer, ultrasonic, diagnostic

Public Device Record Key

3ae590d9-50df-4432-96e8-d33113e29a32

Public Version Date

July 06, 2018

Public Version Number

4

DI Record Publish Date

March 08, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-