Clearance Summary
PACEART TX3 CARDIAC EVENT RECORDER received FDA 510(k) clearance under submission number K012407, sponsored by Paceart, 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 2001-08-14.
- Submission: K012407
- Applicant / Sponsor: Paceart, Inc.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2920
- Decision date: 2001-08-14
Classification & Regulation
This clearance is catalogued under FDA product code DXH and 21 CFR 870.2920, within the Cardiovascular review panel as a Class II device.