Clearance Summary
HP VIRIDIA COMPONENT MONITORING SYSTEM, MODEL REV. K received FDA 510(k) clearance under submission number K990125, sponsored by Hewlett-Packard GmbH. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1999-01-29.
- Submission: K990125
- Applicant / Sponsor: Hewlett-Packard GmbH
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1025
- Decision date: 1999-01-29
Classification & Regulation
This clearance is catalogued under FDA product code DSI and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.