FDA 510(k)

Telescope Guide Extension Catheter

K-Number: K252390 · 2025-10-29

Decision Date2025-10-29

Product CodeDQY

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

Telescope Guide Extension Catheter is a medical device manufactured by Medtronic, Ireland. It received FDA 510(k) clearance on 2025-10-29 under approval number K252390. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Telescope Guide Extension Catheter?

Telescope Guide Extension Catheter is a medical device that received FDA 510(k) clearance on 2025-10-29. It is manufactured by Medtronic, Ireland. The 510(k) number is K252390.

When was Telescope Guide Extension Catheter approved by the FDA?

Telescope Guide Extension Catheter received FDA 510(k) clearance on 2025-10-29, under approval number K252390.

What company makes Telescope Guide Extension Catheter?

Telescope Guide Extension Catheter is manufactured by Medtronic, Ireland.

What is the FDA product code for Telescope Guide Extension Catheter?

The FDA product code for Telescope Guide Extension Catheter is DQY.

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Other Devices by Medtronic, Ireland

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Related Devices (Code: DQY)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.