Clearance Summary
BPro BT Ambulatory Blood Pressure Monitoring System with BProSoft BT PC Software received FDA 510(k) clearance under submission number K173028, sponsored by Healthstats International Pte. , Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2018-06-21.
- Submission: K173028
- Applicant / Sponsor: Healthstats International Pte. , Ltd.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1130
- Decision date: 2018-06-21
Classification & Regulation
This clearance is catalogued under FDA product code DXN and 21 CFR 870.1130, within the Cardiovascular review panel as a Class II device.