Clearance Summary
WATCH STYLE WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL: KLOCK received FDA 510(k) clearance under submission number K991545, sponsored by Industrielle Entwicklung Medizintechnik Und Vertri. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2000-01-19.
- Submission: K991545
- Applicant / Sponsor: Industrielle Entwicklung Medizintechnik Und Vertri
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1120
- Decision date: 2000-01-19
Classification & Regulation
This clearance is catalogued under FDA product code DXQ and 21 CFR 870.1120, within the Cardiovascular review panel as a Class II device.