Clearance Summary
7 FRENCH DUAL LUMEN COM CENT VEIN CATH SYS received FDA 510(k) clearance under submission number K852791, sponsored by Cardio-Vascular Innovations, 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 1985-11-05.
- Submission: K852791
- Applicant / Sponsor: Cardio-Vascular Innovations, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1250
- Decision date: 1985-11-05
Classification & Regulation
This clearance is catalogued under FDA product code DQY and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.