Class Class II

Telescope Guide Extension Catheter (K252390)

K252390 2025-10-29 Traditional
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Description

Telescope Guide Extension Catheter by Medtronic, Ireland, an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252390
Clearance Date2025-10-29
Clearance TypeTraditional
Product CodeDQY
Regulation Number870.1250

Categories

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