Catalog Number

-

Brand Name

Voluson

Version/Model Number

SWIFT

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

K201828

Product Code

ITX

Product Code Name

Transducer, ultrasonic, diagnostic

Public Device Record Key

8c49b2cd-8ec8-4534-86b6-efc86db9c098

Public Version Date

August 16, 2022

Public Version Number

2

DI Record Publish Date

October 28, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-