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FDA 510(k)

CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set

K-Number: K251828 · 2025-08-22

ApplicantCerenovus, Inc.
Decision Date2025-08-22
Product CodeNRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set is a medical device manufactured by Cerenovus, Inc.. It received FDA 510(k) clearance on 2025-08-22 under approval number K251828. The device is classified under product code NRY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set?

CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set is a medical device that received FDA 510(k) clearance on 2025-08-22. It is manufactured by Cerenovus, Inc.. The 510(k) number is K251828.

When was CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set approved by the FDA?

CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set received FDA 510(k) clearance on 2025-08-22, under approval number K251828.

What company makes CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set?

CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set is manufactured by Cerenovus, Inc..

What is the FDA product code for CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set?

The FDA product code for CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set is NRY.

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 Cerenovus, Inc.

K230726CEREGLIDE 92 Intermediate Catheter K221930CEREGLIDE 71 Intermediate Catheter K221934CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set K241244CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter K241221CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing Set K233982CEREGLIDE 92 Catheter System

View all 9 devices →

Related Devices (Code: NRY)

K161879Solitaire Platinum Revascularization DeviceMicro Therapeutics, Inc. d/b/a ev3 Neurovascular K161640Penumbra System ACE 68 Reperfusion CatheterPenumbra, Inc. K161064Penumbra System ACE 68 Reperfusion CatheterPenumbra, Inc. K160449Penumbra System, Penumbra Pump MAXPenumbra, Inc. K152541Penumbra System ACE 64 and ACE 68 Reperfusion CathetersPenumbra, Inc. K172448Riptide Aspiration SystemMicro Therapeutics, Inc. d/b/a ev3 Neurovascular

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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