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CARDIOSOFT/CASE CARDIAC TESTING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031561
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2003
Days to Decision
74 days
Submission Type
Summary

CARDIOSOFT/CASE CARDIAC TESTING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031561
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2003
Days to Decision
74 days
Submission Type
Summary