510(k) K232816
K232816 is an FDA 510(k) premarket notification submitted by Shenzhen LE Medical Technology Co., Ltd. for the device "Electrocardiograph, model: ECG301". The FDA issued a decision of Substantially Equivalent on June 7, 2024. The device falls under product code DPS (Electrocardiograph), a Class II device regulated under 21 CFR 870.2340.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 7, 2024
- Date Received
- September 13, 2023
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Electrocardiograph
- Device Class
- Class II
- Regulation Number
- 870.2340
- Review Panel
- CV
- Submission Type