Class Class II

mcompass Anorectal Balloon Expulsion Catheter (RMD-003-001) (K252605)

K252605 2025-12-05 Traditional
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Description

mcompass Anorectal Balloon Expulsion Catheter (RMD-003-001) by Medspira, LLC, an FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252605
Clearance Date2025-12-05
Clearance TypeTraditional
Product CodeFFX
Regulation Number876.1725

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