FDA 510(k), K944254, OKTAS STEREO VIEWING SYSTEM
FDA 510(k), K944254, OKTAS STEREO VIEWING SYSTEM
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510(K) Number: K944254
Device Name: OKTAS STEREO VIEWING SYSTEM
Manufacturer:
Device Classification Name: Endoscopic Video Imaging System/Component, Gastroenterology-Urology
Regulation Number: 876.1500
Classification Product Code: FET
Date Received: 08/31/1994
Decision Date: 11/30/1994
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: OKTAS STEREO VIEWING SYSTEM
Manufacturer:
Device Classification Name: Endoscopic Video Imaging System/Component, Gastroenterology-Urology
Regulation Number: 876.1500
Classification Product Code: FET
Date Received: 08/31/1994
Decision Date: 11/30/1994
Regulation Medical Specialty: Gastroenterology/Urology