FDA 510(k), K132839, FUSE 1C COLONOSCOPY SYSTEM
FDA 510(k), K132839, FUSE 1C COLONOSCOPY SYSTEM
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$149.00 USD
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510(K) Number: K132839
Device Name: FUSE 1C COLONOSCOPY SYSTEM
Manufacturer:
Device Classification Name: Colonoscope And Accessories, Flexible/Rigid
Regulation Number: 876.1500
Classification Product Code: FDF
Date Received: 09/10/2013
Decision Date: 02/06/2014
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: FUSE 1C COLONOSCOPY SYSTEM
Manufacturer:
Device Classification Name: Colonoscope And Accessories, Flexible/Rigid
Regulation Number: 876.1500
Classification Product Code: FDF
Date Received: 09/10/2013
Decision Date: 02/06/2014
Regulation Medical Specialty: Gastroenterology/Urology