Clearance Summary
MONITOR, MODEL 2817 received FDA 510(k) clearance under submission number K902334, sponsored by Esaote Biomedica Spa. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1990-06-26.
- Submission: K902334
- Applicant / Sponsor: Esaote Biomedica Spa
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2450
- Decision date: 1990-06-26
Classification & Regulation
This clearance is catalogued under FDA product code DXJ and 21 CFR 870.2450, within the Cardiovascular review panel as a Class II device.