Clearance Summary
MoMe Kardia Wireless Ambulatory ECG Monitoring and Detection System received FDA 510(k) clearance under submission number K160064, sponsored by Infobionic, 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 2016-03-11.
- Submission: K160064
- Applicant / Sponsor: Infobionic, Inc.
- Clearance pathway: Abbreviated
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1025
- Decision date: 2016-03-11
Classification & Regulation
This clearance is catalogued under FDA product code QYX and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.