Class Class II

Vertex(TM) Catheter (K252027)

K252027 2025-09-12 Traditional
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Description

Vertex(TM) Catheter by Jupiter Endovascular, an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252027
Clearance Date2025-09-12
Clearance TypeTraditional
Product CodeDYB
Regulation Number870.1340

Categories

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