Class Class II

DuoprossTM Smart Cap (Type I) (K252518)

K252518 2025-12-17 Traditional
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Description

DuoprossTM Smart Cap (Type I) by Duopross Meditech Corporate, an FDA 510(k) cleared general hospital device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252518
Clearance Date2025-12-17
Clearance TypeTraditional
Product CodeFMF
Regulation Number880.5860

Categories

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