Class Class II

FUJIFILM Endoscope Model EI-740D/S (K221551)

K221551 2023-01-27 Traditional
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Description

FUJIFILM Endoscope Model EI-740D/S by Fujifilm Corporaton — FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK221551
Clearance Date2023-01-27
Clearance TypeTraditional
Product CodeFDS
Regulation Number876.1500

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