Clearance Summary
GUIDING CATHETER (TIP SOFTNESS CHANGE) received FDA 510(k) clearance under submission number K883981, sponsored by Devices For Vascular Intervention, 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 1988-11-03.
- Submission: K883981
- Applicant / Sponsor: Devices For Vascular Intervention, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.4210
- Decision date: 1988-11-03
Classification & Regulation
This clearance is catalogued under FDA product code DWF and 21 CFR 870.4210, within the Cardiovascular review panel as a Class II device.