Clearance Summary
TEMPUS IC PROFESSIONAL PATIENT MONITOR received FDA 510(k) clearance under submission number K101264, sponsored by Remote Diagnostic Technologies , 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 2010-05-11.
- Submission: K101264
- Applicant / Sponsor: Remote Diagnostic Technologies , Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2300
- Decision date: 2010-05-11
Classification & Regulation
This clearance is catalogued under FDA product code MWI and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.