Clearance Summary
Q4000 AND Q3040 ELECTROCARDIOGRAPH MONITOR received FDA 510(k) clearance under submission number K863159, sponsored by Quinton, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1986-10-06.
- Submission: K863159
- Applicant / Sponsor: Quinton, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1025
- Decision date: 1986-10-06
Classification & Regulation
This clearance is catalogued under FDA product code DSI and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.