Clearance Summary
LUCON M-SERIES PATIENT MONITOR, MODELS M20 AND M30 received FDA 510(k) clearance under submission number K100217, sponsored by Mediana Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2010-06-08.
- Submission: K100217
- Applicant / Sponsor: Mediana Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1025
- Decision date: 2010-06-08
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.