Class Class II

SurfRider 13 Microcatheter (K251668)

K251668 2026-01-05 Traditional
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Description

SurfRider 13 Microcatheter by Kaneka Americas Holding, Inc., an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251668
Clearance Date2026-01-05
Clearance TypeTraditional
Product CodeQJP
Regulation Number870.1250

Categories

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