FDA 510(k), K030940, NOMAD ND1000M AUGMENTED VISION SYSTEM

FDA 510(k), K030940, NOMAD ND1000M AUGMENTED VISION SYSTEM

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510(K) Number: K030940
Device Name: NOMAD ND1000M AUGMENTED VISION SYSTEM
Manufacturer:
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 03/25/2003
Decision Date: 04/09/2003
Regulation Medical Specialty: Gastroenterology/Urology
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