Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Indigo System Aspiration Catheter 7, Indigo Aspiration System Separator 7, Lightning 7

K-Number: K210083 · 2021-02-09

ApplicantPenumbra, Inc.
Decision Date2021-02-09
Product CodeQEW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Indigo System Aspiration Catheter 7, Indigo Aspiration System Separator 7, Lightning 7 is a medical device manufactured by Penumbra, Inc.. It received FDA 510(k) clearance on 2021-02-09 under approval number K210083. 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 System Aspiration Catheter 7, Indigo Aspiration System Separator 7, Lightning 7?

Indigo System Aspiration Catheter 7, Indigo Aspiration System Separator 7, Lightning 7 is a medical device that received FDA 510(k) clearance on 2021-02-09. It is manufactured by Penumbra, Inc.. The 510(k) number is K210083.

When was Indigo System Aspiration Catheter 7, Indigo Aspiration System Separator 7, Lightning 7 approved by the FDA?

Indigo System Aspiration Catheter 7, Indigo Aspiration System Separator 7, Lightning 7 received FDA 510(k) clearance on 2021-02-09, under approval number K210083.

What company makes Indigo System Aspiration Catheter 7, Indigo Aspiration System Separator 7, Lightning 7?

Indigo System Aspiration Catheter 7, Indigo Aspiration System Separator 7, Lightning 7 is manufactured by Penumbra, Inc..

What is the FDA product code for Indigo System Aspiration Catheter 7, Indigo Aspiration System Separator 7, Lightning 7?

The FDA product code for Indigo System Aspiration Catheter 7, Indigo Aspiration System Separator 7, Lightning 7 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)

View all 59 devices →

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.

↑