Clearance Summary
Tempus Pro Patient Monitor received FDA 510(k) clearance under submission number K201746, sponsored by Remote Diagnostic Technologies Limited. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2020-09-18.
- Submission: K201746
- Applicant / Sponsor: Remote Diagnostic Technologies Limited
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1025
- Decision date: 2020-09-18
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.