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FDA 510(k)

Radical the Dude 7F Guide Catheter

K-Number: K231393 · 2023-11-30

Decision Date2023-11-30
Product CodeQJP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Radical the Dude 7F Guide Catheter is a medical device manufactured by Maduro Medical, Inc.. It received FDA 510(k) clearance on 2023-11-30 under approval number K231393. 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 Radical the Dude 7F Guide Catheter?

Radical the Dude 7F Guide Catheter is a medical device that received FDA 510(k) clearance on 2023-11-30. It is manufactured by Maduro Medical, Inc.. The 510(k) number is K231393.

When was Radical the Dude 7F Guide Catheter approved by the FDA?

Radical the Dude 7F Guide Catheter received FDA 510(k) clearance on 2023-11-30, under approval number K231393.

What company makes Radical the Dude 7F Guide Catheter?

Radical the Dude 7F Guide Catheter is manufactured by Maduro Medical, Inc..

What is the FDA product code for Radical the Dude 7F Guide Catheter?

The FDA product code for Radical the Dude 7F Guide Catheter is QJP.

Related Clinical Trials

Other Devices by Maduro Medical, Inc.

Related Devices (Code: QJP)

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.