Class Class II

Kodiak™ Dual Port Coaxial Introducer Kit (K230631)

K230631 2023-05-22 Traditional
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Description

Kodiak™ Dual Port Coaxial Introducer Kit by Argon Medical Devices — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230631
Clearance Date2023-05-22
Clearance TypeTraditional
Product CodeDYB
Regulation Number870.1340

Categories

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