510(k) K251751
K251751 is an FDA 510(k) premarket notification submitted by Shenzhen Ykd Technology Co., Ltd. for the device "Spo2 Sensor CSS032D". The FDA issued a decision of Substantially Equivalent on December 19, 2025. The device falls under product code DQA (Oximeter), a Class II device regulated under 21 CFR 870.2700.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 19, 2025
- Date Received
- June 9, 2025
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Oximeter
- Device Class
- Class II
- Regulation Number
- 870.2700
- Review Panel
- AN
- Submission Type