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FDA 510(k)

Indigo® Lightning Flash Aspiration System – Select +™ Catheter

K-Number: K241399 · 2024-06-10

ApplicantPenumbra, Inc.
Decision Date2024-06-10
Product CodeQEW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Indigo® Lightning Flash Aspiration System – Select +™ Catheter is a medical device manufactured by Penumbra, Inc.. It received FDA 510(k) clearance on 2024-06-10 under approval number K241399. 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 Indigo® Lightning Flash Aspiration System – Select +™ Catheter?

Indigo® Lightning Flash Aspiration System – Select +™ Catheter is a medical device that received FDA 510(k) clearance on 2024-06-10. It is manufactured by Penumbra, Inc.. The 510(k) number is K241399.

When was Indigo® Lightning Flash Aspiration System – Select +™ Catheter approved by the FDA?

Indigo® Lightning Flash Aspiration System – Select +™ Catheter received FDA 510(k) clearance on 2024-06-10, under approval number K241399.

What company makes Indigo® Lightning Flash Aspiration System – Select +™ Catheter?

Indigo® Lightning Flash Aspiration System – Select +™ Catheter is manufactured by Penumbra, Inc..

What is the FDA product code for Indigo® Lightning Flash Aspiration System – Select +™ Catheter?

The FDA product code for Indigo® Lightning Flash Aspiration System – Select +™ Catheter is QEW.

Related Clinical Trials

NCT07475091 Standardizing Swallow Pressure Measurements NOT_YET_RECRUITING NCT05003843 BOLT: Study of the Indigo® Aspiration System When Used in Patients With Deep Vein Thrombosis ACTIVE_NOT_RECRUITING NCT06510556 Feasibility Study of the FARAFLEX Mapping and PFA System RECRUITING NCT06735534 Repeat Ablation of Persistent Atrial Fibrillation, Including Mitral Isthmus Catheter Ablation, With the FARAPULSE Pulsed Field Ablation System RECRUITING NCT07095660 RECANA OUS - Recana Thrombectomy Catheter System for Venous Obstruction and Occlusion Study (RECANA-OUS-IRL) RECRUITING NCT03053141 RHythmia mAPping and Signal acquisitiOn for Data analYsis (RHAPSODY) RECRUITING

Other Devices by Penumbra, Inc.

K161506Penumbra Aspiration System K161640Penumbra System ACE 68 Reperfusion Catheter K161523INDIGO Aspiration System K161064Penumbra System ACE 68 Reperfusion Catheter K160449Penumbra System, Penumbra Pump MAX K160533Penumbra Embolectomy Aspiration System (INDIGOTM Aspiration System)

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Related Devices (Code: QEW)

K162970FlowTriever Retrieval/Aspiration System, Aspiration Guide Catheter, Retraction AspiratorInari Medical K161506Penumbra Aspiration SystemPenumbra, Inc. K161523INDIGO Aspiration SystemPenumbra, Inc. K160533Penumbra Embolectomy Aspiration System (INDIGOTM Aspiration System)Penumbra, Inc. K173470ClotTriever Thrombectomy System, ClotTriever Catheter, ClotTriever SheathInari Medical K163549ClotTriever Thrombectomy SystemInari Medical, Inc.

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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