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Ellipsys Vascular Access System (Ellipsys System), (Power Controller Model No. AMI-1001 & Catheter & Needle Model No. AMI-6005)

K181725 Class II Traditional
Decision Date
2018-10-05
Sponsor / Applicant
Avenu Medical, Inc.

Technical Specification

510(k) Submission ID K181725
Product Code PQK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1252
Decision Date 2018-10-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Ellipsys Vascular Access System (Ellipsys System), (Power Controller Model No. AMI-1001 & Catheter & Needle Model No. AMI-6005) received FDA 510(k) clearance under submission number K181725, sponsored by Avenu Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2018-10-05.

Classification & Regulation

This clearance is catalogued under FDA product code PQK and 21 CFR 870.1252, within the Cardiovascular review panel as a Class II device.