Clearance Summary
MC3 QuickFlow Dual Lumen Catheter received FDA 510(k) clearance under submission number K171610, sponsored by Mc3 Incorporated. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2017-11-16.
- Submission: K171610
- Applicant / Sponsor: Mc3 Incorporated
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.4100
- Decision date: 2017-11-16
Classification & Regulation
This clearance is catalogued under FDA product code PZS and 21 CFR 870.4100, within the Cardiovascular review panel as a Class II device.