Class Class II

Amplatzer Guidewire (K250031)

K250031 2025-10-03 Traditional
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Description

Amplatzer Guidewire by Abbott Medical, an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250031
Clearance Date2025-10-03
Clearance TypeTraditional
Product CodeDQX
Regulation Number870.1330

Categories

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