Clearance Summary
Spo2 Sensor CSS032D received FDA 510(k) clearance under submission number K251751, sponsored by Shenzhen Ykd Technology 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 2025-12-19.
- Submission: K251751
- Applicant / Sponsor: Shenzhen Ykd Technology Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2700
- Decision date: 2025-12-19
Classification & Regulation
This clearance is catalogued under FDA product code DQA and 21 CFR 870.2700, within the Cardiovascular review panel as a Class II device.