SENSICARDIAC MOBI DIAGNOSTIC HEART MURMUR APPLICATION— 510(k) K131044

Substantially Equivalent

Diacoustic Medical Devices (Pty) , Ltd.

FDA 510(k) clearance K131044 for SENSICARDIAC MOBI DIAGNOSTIC HEART MURMUR APPLICATION, Substantially Equivalent on 2013-09-04. Applicant: Diacoustic Medical Devices (Pty) , Ltd..

Clearance details

Applicant: Diacoustic Medical Devices (Pty) , Ltd.
Product code: Code DQD
Advisory panel: Cardiovascular
Date received: 2013-04-15
Decision date: 2013-09-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Crofton, MD, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.