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HEARTEVENT, MODEL AT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072385
510(k) Type
Traditional
Applicant
Diagnostic Devices Pty, Ltd.
Country
Australia
FDA Decision
Substantially Equivalent
Decision Date
1/11/2008
Days to Decision
140 days
Submission Type
Summary

HEARTEVENT, MODEL AT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072385
510(k) Type
Traditional
Applicant
Diagnostic Devices Pty, Ltd.
Country
Australia
FDA Decision
Substantially Equivalent
Decision Date
1/11/2008
Days to Decision
140 days
Submission Type
Summary