FDA 510(k), K000669, MEDIVISION I-VIEW PERSONAL VIDEO DISPLAY

FDA 510(k), K000669, MEDIVISION I-VIEW PERSONAL VIDEO DISPLAY

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510(K) Number: K000669
Device Name: MEDIVISION I-VIEW PERSONAL VIDEO DISPLAY
Manufacturer:
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 02/28/2000
Decision Date: 05/26/2000
Regulation Medical Specialty: Gastroenterology/Urology
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