Clearance Summary
LUX-Dx Insertable Cardiac Monitor, myLUX Software Mobile Application, LUX-Dx Clinic Assistant Software, Application Server Device Services (DS) - US received FDA 510(k) clearance under submission number K193473, sponsored by Boston Scientific Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2020-06-26.
- Submission: K193473
- Applicant / Sponsor: Boston Scientific Corporation
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1025
- Decision date: 2020-06-26
Classification & Regulation
This clearance is catalogued under FDA product code MXD and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.