Catalog Number

-

Brand Name

Versana

Version/Model Number

Active

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

K191798

Product Code

ITX

Product Code Name

Transducer, ultrasonic, diagnostic

Public Device Record Key

20a5cfc0-4d36-46cb-8cef-ed2d1d9cc730

Public Version Date

September 04, 2019

Public Version Number

1

DI Record Publish Date

August 27, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-