Clearance Summary
DYNAMIC ECG SYSTEM MODEL TLC5000 received FDA 510(k) clearance under submission number K101273, sponsored by Contec Medical System Co., 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 2011-09-30.
- Submission: K101273
- Applicant / Sponsor: Contec Medical System Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2800
- Decision date: 2011-09-30
Classification & Regulation
This clearance is catalogued under FDA product code MLO and 21 CFR 870.2800, within the Cardiovascular review panel as a Class II device.