Clearance Summary
.014 HI-TORQUE FLOPPY PATHFINDER GUIDE WIRE received FDA 510(k) clearance under submission number K913631, sponsored by Advanced Cardiovascular Systems, 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 1991-10-28.
- Submission: K913631
- Applicant / Sponsor: Advanced Cardiovascular Systems, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1330
- Decision date: 1991-10-28
Classification & Regulation
This clearance is catalogued under FDA product code DQX and 21 CFR 870.1330, within the Cardiovascular review panel as a Class II device.