Class Class II

Arrow® Nitinol Wire (K241784)

K241784 2024-09-18 Traditional
Home/ Devices/ Arrow® Nitinol Wire (K241784)

Description

Arrow® Nitinol Wire by Teleflex Medical — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241784
Clearance Date2024-09-18
Clearance TypeTraditional
Product CodeDQX
Regulation Number870.1330

Categories

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