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FDA 510(k)

Echo Intracranial Base Catheter

K-Number: K241637 · 2024-12-19

ApplicantStryker Neurovascular
Decision Date2024-12-19
Product CodeQJP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Echo Intracranial Base Catheter is a medical device manufactured by Stryker Neurovascular. It received FDA 510(k) clearance on 2024-12-19 under approval number K241637. The device is classified under product code QJP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Echo Intracranial Base Catheter?

Echo Intracranial Base Catheter is a medical device that received FDA 510(k) clearance on 2024-12-19. It is manufactured by Stryker Neurovascular. The 510(k) number is K241637.

When was Echo Intracranial Base Catheter approved by the FDA?

Echo Intracranial Base Catheter received FDA 510(k) clearance on 2024-12-19, under approval number K241637.

What company makes Echo Intracranial Base Catheter?

Echo Intracranial Base Catheter is manufactured by Stryker Neurovascular.

What is the FDA product code for Echo Intracranial Base Catheter?

The FDA product code for Echo Intracranial Base Catheter is QJP.

Related Clinical Trials

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Official Source

View on FDA Database →

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

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