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EchoGo Core

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191171
510(k) Type
Traditional
Applicant
Ultromics, Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
11/13/2019
Days to Decision
196 days
Submission Type
Summary

EchoGo Core

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191171
510(k) Type
Traditional
Applicant
Ultromics, Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
11/13/2019
Days to Decision
196 days
Submission Type
Summary