FDA 510(k), K153548, VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM

FDA 510(k), K153548, VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM

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510(K) Number: K153548
Device Name: VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM
Manufacturer:
Device Classification Name: Arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 12/11/2015
Decision Date: 02/22/2016
Regulation Medical Specialty: Orthopedic
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