Clearance Summary
Non-invasive Hemodynamic Blood Pressure Monitor received FDA 510(k) clearance under submission number K190893, sponsored by Vita-Course Technologies Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2019-08-07.
- Submission: K190893
- Applicant / Sponsor: Vita-Course Technologies Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1130
- Decision date: 2019-08-07
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.