Clearance Summary
QUINTON Q-CATH, MODEL 000460 received FDA 510(k) clearance under submission number K021906, sponsored by Quinton, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2002-09-04.
- Submission: K021906
- Applicant / Sponsor: Quinton, Inc.
- Clearance pathway: Abbreviated
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1425
- Decision date: 2002-09-04
Classification & Regulation
This clearance is catalogued under FDA product code DQK and 21 CFR 870.1425, within the Cardiovascular review panel as a Class II device.