Last synced on 25 January 2026 at 3:41 am

SENSICARDIAC MOBI DIAGNOSTIC HEART MURMUR APPLICATION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131044
510(k) Type
Traditional
Applicant
Diacoustic Medical Devices (Pty) , Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/2013
Days to Decision
142 days
Submission Type
Summary

SENSICARDIAC MOBI DIAGNOSTIC HEART MURMUR APPLICATION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131044
510(k) Type
Traditional
Applicant
Diacoustic Medical Devices (Pty) , Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/2013
Days to Decision
142 days
Submission Type
Summary