FDA 510(k), K970369, VISTA MINI CAMERA SYSTEM
FDA 510(k), K970369, VISTA MINI CAMERA SYSTEM
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$149.00 USD
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510(K) Number: K970369
Device Name: VISTA MINI CAMERA SYSTEM
Manufacturer:
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 01/31/1997
Decision Date: 04/14/1997
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: VISTA MINI CAMERA SYSTEM
Manufacturer:
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 01/31/1997
Decision Date: 04/14/1997
Regulation Medical Specialty: Gastroenterology/Urology