Clearance Summary
CATHSCANNER(R) VISIONS(TM) 3.5F 54700/5.0F 54600 received FDA 510(k) clearance under submission number K911384, sponsored by Endosonics Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1991-06-25.
- Submission: K911384
- Applicant / Sponsor: Endosonics Corp.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2330
- Decision date: 1991-06-25
Classification & Regulation
This clearance is catalogued under FDA product code DXK and 21 CFR 870.2330, within the Cardiovascular review panel as a Class II device.