Catalog Number

Voluson-Signature-to-BT22-UPG

Brand Name

Voluson

Version/Model Number

Signature to BT22 UPG

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

K180374,K213642

Product Code

IYN

Product Code Name

System, imaging, pulsed doppler, ultrasonic

Public Device Record Key

2dd5a7b0-54af-4bfb-9f95-6a998d4d56fb

Public Version Date

February 04, 2022

Public Version Number

2

DI Record Publish Date

December 14, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-