Clearance Summary
IVT 0.014 GUIDE WIRE received FDA 510(k) clearance under submission number K895903, sponsored by Intensive Technology, 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 1990-01-04.
- Submission: K895903
- Applicant / Sponsor: Intensive Technology, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1330
- Decision date: 1990-01-04
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.