Clearance Summary
PERCUSURGE GUARDWIRE TEMPORARY OCCLUSION AND ASPIRATION SYSTEM received FDA 510(k) clearance under submission number K003992, sponsored by Percu Surge, 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 2001-06-01.
- Submission: K003992
- Applicant / Sponsor: Percu Surge, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1250
- Decision date: 2001-06-01
Classification & Regulation
This clearance is catalogued under FDA product code NFA and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.