Clearance Summary
NIHON KOHDEN BEDSIDE MONITOR, MODEL BSM-6000S SERIES received FDA 510(k) clearance under submission number K080342, sponsored by Nihon Kohden America, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2008-02-26.
- Submission: K080342
- Applicant / Sponsor: Nihon Kohden America, Inc.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1025
- Decision date: 2008-02-26
Classification & Regulation
This clearance is catalogued under FDA product code MHX and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.