Clearance Summary
FLEX Vessel Prep System received FDA 510(k) clearance under submission number K202187, sponsored by Venturemed Group, 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 2020-09-11.
- Submission: K202187
- Applicant / Sponsor: Venturemed Group, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1250
- Decision date: 2020-09-11
Classification & Regulation
This clearance is catalogued under FDA product code PNO and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.