Clearance Summary
HYBRID PERIPHERAL DILATION CATHETER received FDA 510(k) clearance under submission number K834220, sponsored by American Edwards Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1984-01-27.
- Submission: K834220
- Applicant / Sponsor: American Edwards Laboratories
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1250
- Decision date: 1984-01-27
Classification & Regulation
This clearance is catalogued under FDA product code LIT and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.