Clearance Summary
Ellipsys Vascular Access System (Ellipsys System), Power Controller, Ellipsys Vascular Access System (Ellipsys System), Catheter, Ellipsys Vascular Access System (Ellipsys System), Needle received FDA 510(k) clearance under submission number K191114, sponsored by Avenu Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2019-08-09.
- Submission: K191114
- Applicant / Sponsor: Avenu Medical
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1252
- Decision date: 2019-08-09
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.