FDA 510(k), K042076, FUJINON G5 DUODENSCOPES; G5 DUODENOSCOPES, ED-450XT5, ED-250XT5

FDA 510(k), K042076, FUJINON G5 DUODENSCOPES; G5 DUODENOSCOPES, ED-450XT5, ED-250XT5

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510(K) Number: K042076
Device Name: FUJINON G5 DUODENSCOPES; G5 DUODENOSCOPES, ED-450XT5, ED-250XT5
Manufacturer:
Device Classification Name: Duodenoscope And Accessories, Flexible/Rigid
Regulation Number: 876.1500
Classification Product Code: FDT
Date Received: 08/02/2004
Decision Date: 11/18/2004
Regulation Medical Specialty: Gastroenterology/Urology
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