Clearance Summary
QUICKCAT EXTRACTION CATHETER, MODEL 60090-01 received FDA 510(k) clearance under submission number K073519, sponsored by Kensey Nash Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2008-03-28.
- Submission: K073519
- Applicant / Sponsor: Kensey Nash Corp.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.5150
- Decision date: 2008-03-28
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.