Clearance Summary
HEART RATE TURBULENCE ANALYSIS TECHNOLOGIES received FDA 510(k) clearance under submission number K042148, sponsored by Ge Medical Syst. Information Technologies. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2004-12-03.
- Submission: K042148
- Applicant / Sponsor: Ge Medical Syst. Information Technologies
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1425
- Decision date: 2004-12-03
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.