Diacoustic Medical Devices (Pty) , Ltd.
2 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| SENSICARDIAC MOBI DIAGNOSTIC HEART MURMUR APPLICATION (K131044) | Diacoustic Medical Devices (Pty) , Ltd. | 2013-09-04 |
| SENSI (K110704) | Diacoustic Medical Devices (Pty) , Ltd. | 2011-06-24 |
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