Catalog Number

-

Brand Name

Vivid

Version/Model Number

E v202 to v203 UPG

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K181685

Product Code

ITX

Product Code Name

Transducer, ultrasonic, diagnostic

Public Device Record Key

6e2cd2a8-3263-4973-a59b-d5b7e999a2a0

Public Version Date

December 14, 2018

Public Version Number

1

DI Record Publish Date

November 13, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-