Catalog Number

-

Brand Name

EchoGo

Version/Model Number

Core 2.0

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

K213275

Product Code

QIH

Product Code Name

Automated Radiological Image Processing Software

Public Device Record Key

747d36f5-7f8c-4ea4-b089-dfa3fcdf2265

Public Version Date

January 27, 2022

Public Version Number

1

DI Record Publish Date

January 19, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-