K232816
- 510(k) number
- K232816
- Device name
- Electrocardiograph, model: ECG301
- Applicant
- Shenzhen LE Medical Technology Co., Ltd. CN
- Product code
- DPS — Electrocardiograph
- Decision date
- 2024-06-07
- Date received
- 2023-09-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K232816.pdf
Official FDA record: K232816
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.