Class Class II

Resitu Slider 09 (RESL09) (K252183)

K252183 2025-09-24 Traditional
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Description

Resitu Slider 09 (RESL09) by Resitu Medical AB, an FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252183
Clearance Date2025-09-24
Clearance TypeTraditional
Product CodeKNW
Regulation Number876.1075

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