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HEARTEVENT, MODEL AT

Page Type
Cleared 510(K)
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)
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