Class Class II

FUJIFILM Stiffening Wire Device (SW-2000) (K251204)

K251204 2025-09-26 Traditional
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Description

FUJIFILM Stiffening Wire Device (SW-2000) by Fujifilm Healthcare Americas Corporation, an FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251204
Clearance Date2025-09-26
Clearance TypeTraditional
Product CodeFDA
Regulation Number876.1500

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