Clearance Summary
Dyna-Vision Telemonitoring System received FDA 510(k) clearance under submission number K152973, sponsored by Techmedic Development International B.V.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2016-04-29.
- Submission: K152973
- Applicant / Sponsor: Techmedic Development International B.V.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1025
- Decision date: 2016-04-29
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.