Clearance Summary
ANGIOJET ULTRA DVX THROMBECTOMY SET received FDA 510(k) clearance under submission number K113428, sponsored by Medrad, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2011-12-02.
- Submission: K113428
- Applicant / Sponsor: Medrad, Inc.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.5150
- Decision date: 2011-12-02
Classification & Regulation
This clearance is catalogued under FDA product code QEZ and 21 CFR 870.5150, within the Cardiovascular review panel as a Class II device.