Clearance Summary
MICROLIFE WRIST WATCH BLOOD PRESSURE MONITOR, MODEL BP-3BU1 received FDA 510(k) clearance under submission number K001182, sponsored by Microlife Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2000-08-01.
- Submission: K001182
- Applicant / Sponsor: Microlife Corp.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1130
- Decision date: 2000-08-01
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.