Clearance Summary
BZ-576 NON-INVASIVE AUTOMATIC BLOOD PRESSURE MONITOR received FDA 510(k) clearance under submission number K033216, sponsored by The Buzz Group, LLC. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2004-05-04.
- Submission: K033216
- Applicant / Sponsor: The Buzz Group, LLC
- Clearance pathway: Abbreviated
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1130
- Decision date: 2004-05-04
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.