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FDA 510(k)

Excipio LV Thrombectomy Device

K-Number: K223897 · 2023-02-17

Decision Date2023-02-17
Product CodeQEW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Excipio LV Thrombectomy Device is a medical device manufactured by Contego Medical, Inc.. It received FDA 510(k) clearance on 2023-02-17 under approval number K223897. The device is classified under product code QEW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Excipio LV Thrombectomy Device?

Excipio LV Thrombectomy Device is a medical device that received FDA 510(k) clearance on 2023-02-17. It is manufactured by Contego Medical, Inc.. The 510(k) number is K223897.

When was Excipio LV Thrombectomy Device approved by the FDA?

Excipio LV Thrombectomy Device received FDA 510(k) clearance on 2023-02-17, under approval number K223897.

What company makes Excipio LV Thrombectomy Device?

Excipio LV Thrombectomy Device is manufactured by Contego Medical, Inc..

What is the FDA product code for Excipio LV Thrombectomy Device?

The FDA product code for Excipio LV Thrombectomy Device is QEW.

Related Clinical Trials

Other Devices by Contego Medical, Inc.

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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.