Clearance Summary
ESSENZ Patient Monitor received FDA 510(k) clearance under submission number K212003, sponsored by Livanova Deutschland, 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 2021-11-10.
- Submission: K212003
- Applicant / Sponsor: Livanova Deutschland, GmbH
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2450
- Decision date: 2021-11-10
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.