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CASE V7.0 Cardiac Testing System and CardioSoft V7.0 Cardiac Testing System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231870
510(k) Type
Traditional
Applicant
GE Medical Systems Information Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2023
Days to Decision
170 days
Submission Type
Summary

CASE V7.0 Cardiac Testing System and CardioSoft V7.0 Cardiac Testing System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231870
510(k) Type
Traditional
Applicant
GE Medical Systems Information Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2023
Days to Decision
170 days
Submission Type
Summary