Clearance Summary
SURGI-VISION GUIDEWIRE COIL received FDA 510(k) clearance under submission number K003436, sponsored by Surgi-Vision, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2001-02-02.
- Submission: K003436
- Applicant / Sponsor: Surgi-Vision, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1000
- Decision date: 2001-02-02
Classification & Regulation
This clearance is catalogued under FDA product code MOS and 21 CFR 892.1000, within the Radiology review panel as a Class II device.