FDA 510(k) Applications Submitted by DIACOUSTIC MEDICAL DEVICES (PTY) LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K110704 03/14/2011 SENSI DIACOUSTIC MEDICAL DEVICES (PTY) LTD.
K131044 04/15/2013 SENSICARDIAC MOBI DIAGNOSTIC HEART MURMUR APPLICATION DIACOUSTIC MEDICAL DEVICES (PTY) LTD.


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