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Ellipsys Vascular Access System (Ellipsys System), Power Controller, Ellipsys Vascular Access System (Ellipsys System), Catheter, Ellipsys Vascular Access System (Ellipsys System), Crossing Needle

K183615 Class II Special
Decision Date
2019-01-25
Sponsor / Applicant
Avenu Medical, Inc.

Technical Specification

510(k) Submission ID K183615
Product Code PQK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1252
Decision Date 2019-01-25
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Ellipsys Vascular Access System (Ellipsys System), Power Controller, Ellipsys Vascular Access System (Ellipsys System), Catheter, Ellipsys Vascular Access System (Ellipsys System), Crossing Needle received FDA 510(k) clearance under submission number K183615, sponsored by Avenu Medical, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2019-01-25.

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.