Clearance Summary
TRULY AUTOMATIC BLOOD PRESSURE MONITOR, MODEL DB11 received FDA 510(k) clearance under submission number K081852, sponsored by Truly Instrument Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2008-12-12.
- Submission: K081852
- Applicant / Sponsor: Truly Instrument Limited
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1130
- Decision date: 2008-12-12
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.