Clearance Summary
EZYPRO ECG Recorder (Model: UG02) received FDA 510(k) clearance under submission number K213233, sponsored by Sigknow Biomedical 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 2022-06-23.
- Submission: K213233
- Applicant / Sponsor: Sigknow Biomedical Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2910
- Decision date: 2022-06-23
Classification & Regulation
This clearance is catalogued under FDA product code DRG and 21 CFR 870.2910, within the Cardiovascular review panel as a Class II device.