Class Class II

DIASAFEplusUS (F00013010) (K251851)

K251851 2025-10-09 Traditional
Home/ Devices/ DIASAFEplusUS (F00013010) (K251851)

Description

DIASAFEplusUS (F00013010) by Fresenius Medical Care Renal Therapies Group, LLC, an FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251851
Clearance Date2025-10-09
Clearance TypeTraditional
Product CodeFIP
Regulation Number876.5665

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