FDA 510(k), K062481, SERENO ELECTRONIC STETHOSCOPE

FDA 510(k), K062481, SERENO ELECTRONIC STETHOSCOPE

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510(K) Number: K062481
Device Name: SERENO ELECTRONIC STETHOSCOPE
Manufacturer:
Device Classification Name: Stethoscope, Electronic
Regulation Number: 870.1875
Classification Product Code: DQD
Date Received: 08/24/2006
Decision Date: 10/16/2006
Regulation Medical Specialty: Cardiovascular
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